A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698066



Internal ID15434718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:117289550..117301629hg38UCSC Ensembl
Innerchr1:117832172..117844251hg19UCSC Ensembl
Innerchr1:117633695..117645774hg18UCSC Ensembl
Innerchr1:117544214..117556293hg17UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3812080
hg1912080
hg1812080
hg1712080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521455
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698066
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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