A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705577



Internal ID15442229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:120902325..120916322hg38UCSC Ensembl
Innerchr8:121914565..121928562hg19UCSC Ensembl
Innerchr8:121983746..121997743hg18UCSC Ensembl
Innerchr8:121983746..121997743hg17UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3813998
hg1913998
hg1813998
hg1713998
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528893
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705577
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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