A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643786



Internal ID6683856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15992354..15995304hg38UCSC Ensembl
Innerchr19:15992356..15995303hg38UCSC Ensembl
Outerchr19:15992353..15995306hg38UCSC Ensembl
chr19:16103164..16106114hg19UCSC Ensembl
Innerchr19:16103166..16106113hg19UCSC Ensembl
Outerchr19:16103163..16106116hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382951
hg192951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002706, essv16002700, essv16002698, essv16002704, essv16002707, essv16002695, essv16002702, essv16002687, essv16002699, essv16002703, essv16002694, essv16002688, essv16002691, essv16002692, essv16002696, essv16002705, essv16002693, essv16002689, essv16002701, essv16002697, essv16002690
SamplesHG02836, NA18486, HG02888, NA19190, NA12750, HG03199, NA19374, HG03270, HG02570, NA20126, NA19113, NA18853, HG02896, HG01990, NA19375, NA18517, HG01396, HG02611, NA19310, HG01260, NA19093
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643786
Frequency
Sample Size2504
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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