A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016705



Internal ID19105922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21217797..21411325hg38UCSC Ensembl
Innerchr7:21257416..21450943hg19UCSC Ensembl
Innerchr7:21223941..21417468hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38193529
hg19193528
hg18193528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752926
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)nsv1016705
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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