A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891507



Internal ID19185903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:161562..206255hg38UCSC Ensembl
Outerchr9:161562..228301hg38UCSC Ensembl
Innerchr9:161562..206255hg19UCSC Ensembl
Outerchr9:161562..228301hg19UCSC Ensembl
Innerchr9:151562..196255hg18UCSC Ensembl
Outerchr9:151562..218301hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3866740
hg1966740
hg1866740
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781178, essv25788518
Samples
Known GenesC9orf66, CBWD1, DOCK8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891507
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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