A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516015



Internal ID15443072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45653..128206hg38UCSC Ensembl
Innerchr7:45653..128206hg19UCSC Ensembl
Innerchr7:140736..223289hg18UCSC Ensembl
Innerchr7:140736..223289hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3882554
hg1982554
hg1882554
hg1782554
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675776, nssv665738, nssv689865, nssv666682, nssv678519, nssv689083, nssv700553, nssv677203, nssv662667, nssv660096, nssv681903, nssv702187, nssv672336, nssv687306
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516015
Frequency
Sample Size2026
Observed Gain11
Observed Loss3
Observed Complex0
Frequencyn/a


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