A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701339



Internal ID15091305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16021917..16047835hg38UCSC Ensembl
Innerchr1:16348412..16374330hg19UCSC Ensembl
Innerchr1:16220999..16246917hg18UCSC Ensembl
Innerchr1:16093718..16119636hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3825919
hg1925919
hg1825919
hg1725919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517651
Supporting Variants
Samples
Known GenesCLCNKA, CLCNKB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701339
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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