A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515884



Internal ID15442941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:49313068..49391304hg38UCSC Ensembl
Innerchr7:49352664..49430900hg19UCSC Ensembl
Innerchr7:49323210..49401446hg18UCSC Ensembl
Innerchr7:49129925..49208161hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3878237
hg1978237
hg1878237
hg1778237
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665402, nssv665140, nssv704080
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515884
Frequency
Sample Size2026
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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