A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589896



Internal ID16377305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21650901..21670777hg38UCSC Ensembl
Innerchr3:21692393..21712269hg19UCSC Ensembl
Innerchr3:21667397..21687273hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3819877
hg1919877
hg1819877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959920
Samples
Known GenesZNF385D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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