A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525555



Internal ID15452848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44338308..44349020hg38UCSC Ensembl
Innerchr7:44377907..44388619hg19UCSC Ensembl
Innerchr7:44344432..44355144hg18UCSC Ensembl
Innerchr7:44151147..44161859hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3810713
hg1910713
hg1810713
hg1710713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701694
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525555
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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