A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571174



Internal ID16358583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1806439..1851210hg38UCSC Ensembl
Innerchr16:1856440..1901211hg19UCSC Ensembl
Innerchr16:1796441..1841212hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3844772
hg1944772
hg1844772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4857n54
Supporting Variantsnssv852071
Samples
Known GenesFAHD1, HAGH, MEIOB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571174
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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