A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152973



Internal ID15853412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161099011..161169603hg38UCSC Ensembl
Innerchr4:162020163..162090755hg19UCSC Ensembl
Innerchr4:162239613..162310205hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3870593
hg1970593
hg1870593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595943
Supporting Variants
Samples1780854179_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152973
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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