A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521803



Internal ID15449096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126509265..126579712hg38UCSC Ensembl
Innerchr7:126149319..126219766hg19UCSC Ensembl
Innerchr7:125936555..126007002hg18UCSC Ensembl
Innerchr7:125743270..125813717hg17UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3870448
hg1970448
hg1870448
hg1770448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694573
Samples
Known GenesGRM8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521803
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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