A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148922



Internal ID15506622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6627776..6663776hg38UCSC Ensembl
Innerchr16:6677777..6713777hg19UCSC Ensembl
Innerchr16:6617778..6653778hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3836001
hg1936001
hg1836001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571344
Supporting Variants
Samples1780854080_A
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148922
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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