A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061327



Internal ID18803858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21059770..22484758hg38UCSC Ensembl
Innerchr19:21242576..22667560hg19UCSC Ensembl
Innerchr19:21034416..22459400hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381424989
hg191424985
hg181424985
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570584
Samples
Known GenesLINC00664, LOC641367, ZNF100, ZNF208, ZNF257, ZNF429, ZNF43, ZNF430, ZNF431, ZNF493, ZNF676, ZNF708, ZNF714, ZNF729, ZNF738, ZNF98
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061327
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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