A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1085102



Internal ID15938288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62575192..63238576hg38UCSC Ensembl
Innerchr7:62035570..62698954hg19UCSC Ensembl
Innerchr7:61673005..62336389hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38663385
hg19663385
hg18663385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607242
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1085102
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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