A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1007630



Internal ID16301586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135353966..135478875hg38UCSC Ensembl
Innerchr4:136275121..136400030hg19UCSC Ensembl
Innerchr4:136494571..136619480hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38124910
hg19124910
hg18124910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595513
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)nssv1007630
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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