A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783661



Internal ID19164903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149499939..149617179hg38UCSC Ensembl
Innerchr7:149197030..149314270hg19UCSC Ensembl
Innerchr7:148827963..148945203hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38117241
hg19117241
hg18117241
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891233
Supporting Variants
Samples
Known GenesZNF767
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783661
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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