A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1000261



Internal ID16294217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62793760..62809549hg38UCSC Ensembl
Innerchr4:63659478..63675267hg19UCSC Ensembl
Innerchr4:63342073..63357862hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3815790
hg1915790
hg1815790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594337
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)nssv1000261
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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