A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644276



Internal ID6684344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37023082..37025753hg38UCSC Ensembl
Innerchr19:37023122..37025713hg38UCSC Ensembl
Outerchr19:37023042..37025793hg38UCSC Ensembl
chr19:37513984..37516655hg19UCSC Ensembl
Innerchr19:37514024..37516615hg19UCSC Ensembl
Outerchr19:37513944..37516695hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382672
hg192672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16051045, essv16051046
SamplesNA20805, HG02220
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644276
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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