A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063081



Internal ID19152300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12427939..12494286hg38UCSC Ensembl
Innerchr19:12538753..12605100hg19UCSC Ensembl
Innerchr19:12399753..12466100hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3866348
hg1966348
hg1866348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564762
Samples
Known GenesZNF443, ZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063081
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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