A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524408



Internal ID15451701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148964410..148976273hg38UCSC Ensembl
Innerchr7:148661502..148673365hg19UCSC Ensembl
Innerchr7:148292435..148304298hg18UCSC Ensembl
Innerchr7:148099150..148111013hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3811864
hg1911864
hg1811864
hg1711864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700328
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524408
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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