A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589838



Internal ID16030561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16559591..16614824hg38UCSC Ensembl
Innerchr3:16601098..16656331hg19UCSC Ensembl
Innerchr3:16576102..16631335hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3855234
hg1955234
hg1855234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8247n54
Supporting Variantsnssv959846
Samples
Known GenesDAZL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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