A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573471



Internal ID16014194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84864127..84919498hg38UCSC Ensembl
Innerchr16:84897733..84953104hg19UCSC Ensembl
Innerchr16:83455234..83510605hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3855372
hg1955372
hg1855372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862186
Samples
Known GenesCRISPLD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573471
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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