A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959919



Internal ID16253875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21580895..21597323hg38UCSC Ensembl
Innerchr3:21622387..21638815hg19UCSC Ensembl
Innerchr3:21597391..21613819hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3816429
hg1916429
hg1816429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589895
Supporting Variants
Samples
Known GenesZNF385D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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