A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155364



Internal ID15878422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90537591..90592034hg38UCSC Ensembl
Innerchr7:90166905..90221348hg19UCSC Ensembl
Innerchr7:90004841..90059284hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3854444
hg1954444
hg1854444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607790
Supporting Variants
SamplesHGDP01198
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155364
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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