A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790253



Internal ID18817516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64321351..64511352hg38UCSC Ensembl
Innerchr7:63781729..63971730hg19UCSC Ensembl
Innerchr7:63419164..63609165hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38190002
hg19190002
hg18190002
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891131
Supporting Variants
Samples
Known GenesYWHAEP1, ZNF736
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790253
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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