A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643782



Internal ID7030540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15915630..15919700hg38UCSC Ensembl
Innerchr19:15915631..15919699hg38UCSC Ensembl
Outerchr19:15915629..15919701hg38UCSC Ensembl
chr19:16026440..16030510hg19UCSC Ensembl
Innerchr19:16026441..16030509hg19UCSC Ensembl
Outerchr19:16026439..16030511hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg384071
hg194071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002656, essv16002659, essv16002662, essv16002663, essv16002665, essv16002664, essv16002654, essv16002666, essv16002658, essv16002653, essv16002657, essv16002655, essv16002660, essv16002668, essv16002667, essv16002661
SamplesNA18980, HG00634, NA19062, NA18574, HG00543, NA18613, NA20299, NA18531, NA18535, NA18952, HG00707, HG02079, HG02032, NA18989, HG02020, HG02060
Known GenesCYP4F11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643782
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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