A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722782



Internal ID18674377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41916194..41987372hg38UCSC Ensembl
Innerchr19:42420346..42491524hg19UCSC Ensembl
Innerchr19:47112186..47183364hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3871179
hg1971179
hg1871179
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063979
Supporting Variants
Samples
Known GenesATP1A3, RABAC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722782
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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