A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699104



Internal ID15089070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93885772..93920035hg38UCSC Ensembl
Innerchr1:94351328..94385591hg19UCSC Ensembl
Innerchr1:94123916..94158179hg18UCSC Ensembl
Innerchr1:94063349..94097612hg17UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3834264
hg1934264
hg1834264
hg1734264
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523355
Supporting Variants
Samples
Known GenesGCLM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699104
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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