A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571177



Internal ID16011900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1817039..1897015hg38UCSC Ensembl
Innerchr16:1867040..1947016hg19UCSC Ensembl
Innerchr16:1807041..1887017hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3879977
hg1979977
hg1879977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148897, nssv1148896
SamplesHGDP00105, HGDP00102
Known GenesFAHD1, HAGH, LINC00254, MEIOB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571177
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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