A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065384



Internal ID18807915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21066515..21167895hg38UCSC Ensembl
Innerchr19:21249321..21350698hg19UCSC Ensembl
Innerchr19:21041161..21142538hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38101381
hg19101378
hg18101378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570585
Samples
Known GenesZNF431, ZNF714
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065384
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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