A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683268



Internal ID15073234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16041829..16046629hg38UCSC Ensembl
Innerchr1:16368324..16373124hg19UCSC Ensembl
Innerchr1:16240911..16245711hg18UCSC Ensembl
Innerchr1:16113630..16118430hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384801
hg194801
hg184801
hg174801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517651
Supporting Variants
Samples
Known GenesCLCNKB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683268
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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