A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891783



Internal ID18839493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32545115..32621788hg38UCSC Ensembl
Outerchr10:32542994..32621788hg38UCSC Ensembl
Innerchr10:32834043..32910716hg19UCSC Ensembl
Outerchr10:32831922..32910716hg19UCSC Ensembl
Innerchr10:32874049..32950722hg18UCSC Ensembl
Outerchr10:32871928..32950722hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3878795
hg1978795
hg1878795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792496, essv25791966
Samples
Known GenesCCDC7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891783
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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