A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792496



Internal ID18835751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32542994..32621788hg38UCSC Ensembl
Innerchr10:32831922..32910716hg19UCSC Ensembl
Innerchr10:32871928..32950722hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3878795
hg1978795
hg1878795
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891783
Supporting Variants
Samples
Known GenesCCDC7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792496
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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