A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063115



Internal ID18805646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21599302..22345237hg38UCSC Ensembl
Innerchr19:21782104..22528039hg19UCSC Ensembl
Innerchr19:21573944..22319879hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38745936
hg19745936
hg18745936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724325
Samples
Known GenesLOC641367, ZNF100, ZNF208, ZNF257, ZNF43, ZNF676, ZNF729
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063115
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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