A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571639



Internal ID16012362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21611578..21701422hg38UCSC Ensembl
Innerchr16:21622899..21712743hg19UCSC Ensembl
Innerchr16:21530400..21620244hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3889845
hg1989845
hg1889845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv853114
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571639
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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