A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643799



Internal ID7030556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16547736..16549356hg38UCSC Ensembl
Innerchr19:16547737..16549356hg38UCSC Ensembl
Outerchr19:16547736..16549357hg38UCSC Ensembl
chr19:16658547..16660167hg19UCSC Ensembl
Innerchr19:16658548..16660167hg19UCSC Ensembl
Outerchr19:16658547..16660168hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381621
hg191621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002794, essv16002816, essv16002818, essv16002807, essv16002804, essv16002820, essv16002811, essv16002786, essv16002803, essv16002797, essv16002790, essv16002791, essv16002788, essv16002815, essv16002802, essv16002812, essv16002799, essv16002819, essv16002810, essv16002808, essv16002805, essv16002800, essv16002817, essv16002793, essv16002789, essv16002792, essv16002801, essv16002787, essv16002795, essv16002814, essv16002798, essv16002813, essv16002796, essv16002809, essv16002806
SamplesHG02890, NA20321, HG03455, NA19393, HG01971, HG03074, NA19171, NA20320, NA18916, NA19138, NA20287, NA19041, HG02561, HG03225, NA18864, HG03058, HG01879, HG02108, NA19982, HG02307, HG02968, HG02817, NA19113, HG02635, HG01990, NA19454, HG03259, NA19474, NA19185, HG03410, HG03538, HG02855, HG03376, HG02851, NA19153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643799
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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