A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573538



Internal ID16014261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87743983..87813314hg38UCSC Ensembl
Innerchr16:87777589..87846920hg19UCSC Ensembl
Innerchr16:86335090..86404421hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3869332
hg1969332
hg1869332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862324
Samples
Known GenesKLHDC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573538
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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