A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573475



Internal ID16360884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85214718..85270519hg38UCSC Ensembl
Innerchr16:85248324..85304125hg19UCSC Ensembl
Innerchr16:83805825..83861626hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3855802
hg1955802
hg1855802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149343
SamplesHGDP00685
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573475
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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