A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153169



Internal ID15856059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132700517..132782113hg38UCSC Ensembl
Innerchr4:133621672..133703268hg19UCSC Ensembl
Innerchr4:133841122..133922718hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3881597
hg1981597
hg1881597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595463
Supporting Variants
Samples1798860567_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153169
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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