A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25794766



Internal ID18825865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64233851..64529722hg38UCSC Ensembl
Innerchr7:63694229..63990100hg19UCSC Ensembl
Innerchr7:63331664..63627535hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38295872
hg19295872
hg18295872
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891131
Supporting Variants
Samples
Known GenesYWHAEP1, ZNF679, ZNF680, ZNF736
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=60
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25794766
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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