A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018999



Internal ID19108216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54235975..54351633hg38UCSC Ensembl
Innerchr7:54303668..54419326hg19UCSC Ensembl
Innerchr7:54271162..54386820hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38115659
hg19115659
hg18115659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661323
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)nsv1018999
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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