A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1093599



Internal ID15946785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124147619..124423444hg38UCSC Ensembl
Innerchr7:123787673..124063498hg19UCSC Ensembl
Innerchr7:123574909..123850734hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38275826
hg19275826
hg18275826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608338
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)nssv1093599
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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