A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621337



Internal ID7008206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104604904..104617879hg38UCSC Ensembl
chr9:107367185..107380160hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3812976
hg1912976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13591859, essv13591864, essv13591867, essv13591869, essv13591863, essv13591868, essv13591865, essv13591861, essv13591860, essv13591858, essv13591862, essv13591866
SamplesNA18639, HG00327, HG01277, HG03091, NA18642, HG02090, NA18757, HG00336, NA19149, HG00278, HG00310, NA18957
Known GenesOR13C2, OR13C9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621337
Frequency
Sample Size2504
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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