A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697095



Internal ID15087061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14234265..14235175hg38UCSC Ensembl
Innerchr8:14091774..14092684hg19UCSC Ensembl
Innerchr8:14136145..14137055hg18UCSC Ensembl
Innerchr8:14136145..14137055hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38911
hg19911
hg18911
hg17911
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known GenesSGCZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697095
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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