A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697098



Internal ID15433750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:162907367..162913126hg38UCSC Ensembl
Innerchr1:162877157..162882916hg19UCSC Ensembl
Innerchr1:161143781..161149540hg18UCSC Ensembl
Innerchr1:159608815..159614574hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg385760
hg195760
hg185760
hg175760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519874
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697098
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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