A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704094



Internal ID15094060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14796607..14800057hg38UCSC Ensembl
Innerchr8:14654116..14657566hg19UCSC Ensembl
Innerchr8:14698487..14701937hg18UCSC Ensembl
Innerchr8:14698487..14701937hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg383451
hg193451
hg183451
hg173451
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)nssv704094
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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