A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571364



Internal ID16012087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6788397..6964661hg38UCSC Ensembl
Innerchr16:6838398..7014662hg19UCSC Ensembl
Innerchr16:6778399..6954663hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38176265
hg19176265
hg18176265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4893n54
Supporting Variantsnssv1150504
SamplesNINDS_96
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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