A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153613



Internal ID15526973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178842681..178886077hg38UCSC Ensembl
Innerchr5:178269682..178313078hg19UCSC Ensembl
Innerchr5:178202288..178245684hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3843397
hg1943397
hg1843397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600463
Supporting Variants
SamplesHGDP00286
Known GenesZNF354B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153613
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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