A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153603



Internal ID15854730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:146242909..146307732hg38UCSC Ensembl
Innerchr5:145622472..145687295hg19UCSC Ensembl
Innerchr5:145602665..145667488hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3864824
hg1964824
hg1864824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599937
Supporting Variants
Samples1780862304_A
Known GenesRBM27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153603
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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