A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661278



Internal ID18959559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:52851725..52914549hg38UCSC Ensembl
Innerchr7:52919418..52982242hg19UCSC Ensembl
Innerchr7:52886912..52949736hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3862825
hg1962825
hg1862825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017323
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661278
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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