A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083560



Internal ID15936746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44959115..44961619hg38UCSC Ensembl
Innerchr7:44998714..45001218hg19UCSC Ensembl
Innerchr7:44965239..44967743hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382505
hg192505
hg182505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606810
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)nssv1083560
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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