A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527510



Internal ID15108117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43038251..43080331hg38UCSC Ensembl
Innerchr7:43077850..43119930hg19UCSC Ensembl
Innerchr7:43044375..43086455hg18UCSC Ensembl
Innerchr7:42851090..42893170hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3842081
hg1942081
hg1842081
hg1742081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703964
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527510
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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