A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571624



Internal ID16012347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21514167..21728953hg38UCSC Ensembl
Innerchr16:21525488..21740274hg19UCSC Ensembl
Innerchr16:21432989..21647775hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38214787
hg19214787
hg18214787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4944n54
Supporting Variantsnssv853082
Samples
Known GenesIGSF6, METTL9, OTOA, SLC7A5P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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