A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621328



Internal ID7008197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104050448..104090010hg38UCSC Ensembl
Innerchr9:104050453..104090006hg38UCSC Ensembl
Outerchr9:104050444..104090015hg38UCSC Ensembl
chr9:106812729..106852291hg19UCSC Ensembl
Innerchr9:106812734..106852287hg19UCSC Ensembl
Outerchr9:106812725..106852296hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3839563
hg1939563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13591669, essv13591667, essv13591663, essv13591661, essv13591668, essv13591665, essv13591666, essv13591664, essv13591662
SamplesHG03298, NA19171, HG03476, HG01896, NA19035, HG02464, HG03025, HG02462, HG03072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621328
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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