A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1045247



Internal ID15898433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:165768554..165838839hg38UCSC Ensembl
Innerchr5:165195559..165265844hg19UCSC Ensembl
Innerchr5:165128137..165198422hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3870286
hg1970286
hg1870286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600244
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)nssv1045247
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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