A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571248



Internal ID16011971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3034108..3165103hg38UCSC Ensembl
Innerchr16:3084109..3215104hg19UCSC Ensembl
Innerchr16:3024110..3155105hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38130996
hg19130996
hg18130996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852260
Samples
Known GenesCCDC64B, IL32, LOC100128770, MMP25, ZNF205, ZNF205-AS1, ZNF213, ZSCAN10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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