A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023657



Internal ID16317613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2052935..2068636hg38UCSC Ensembl
Innerchr5:2053049..2068750hg19UCSC Ensembl
Innerchr5:2106049..2121750hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3815702
hg1915702
hg1815702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596906
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)nssv1023657
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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