A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664905



Internal ID15054871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22500085..22552644hg38UCSC Ensembl
Innerchr8:22357598..22410157hg19UCSC Ensembl
Innerchr8:22413543..22466102hg18UCSC Ensembl
Innerchr8:22413543..22466102hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3852560
hg1952560
hg1852560
hg1752560
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517680
Supporting Variants
Samples
Known GenesPPP3CC, SORBS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664905
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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