A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597377



Internal ID16384786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18676765..18726907hg38UCSC Ensembl
Innerchr5:18676874..18727016hg19UCSC Ensembl
Innerchr5:18712631..18762773hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3850143
hg1950143
hg1850143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9634n54
Supporting Variantsnssv1152863
Samples1782681169_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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