A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705429



Internal ID15442081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72579475..72609740hg38UCSC Ensembl
Innerchr1:73045158..73075423hg19UCSC Ensembl
Innerchr1:72817746..72848011hg18UCSC Ensembl
Innerchr1:72757179..72787444hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3830266
hg1930266
hg1830266
hg1730266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516582
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705429
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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