A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523402



Internal ID15450695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45140279..45150815hg38UCSC Ensembl
Innerchr7:45179878..45190414hg19UCSC Ensembl
Innerchr7:45146403..45156939hg18UCSC Ensembl
Innerchr7:44953118..44963654hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3810537
hg1910537
hg1810537
hg1710537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699153
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523402
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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