A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597056



Internal ID16384465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8703503..8757929hg38UCSC Ensembl
Innerchr5:8703615..8758041hg19UCSC Ensembl
Innerchr5:8756615..8811041hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3854427
hg1954427
hg1854427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9568n54
Supporting Variantsnssv1024109, nssv1153009
Samples1780854558_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597056
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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