A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680788



Internal ID15070754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16021917..16043720hg38UCSC Ensembl
Innerchr1:16348412..16370215hg19UCSC Ensembl
Innerchr1:16220999..16242802hg18UCSC Ensembl
Innerchr1:16093718..16115521hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821804
hg1921804
hg1821804
hg1721804
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517651
Supporting Variants
Samples
Known GenesCLCNKA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680788
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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