A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567541



Internal ID18519136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41916194..42001892hg38UCSC Ensembl
Innerchr19:42420346..42506044hg19UCSC Ensembl
Innerchr19:47112186..47197884hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3885699
hg1985699
hg1885699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055609
Supporting Variants
Samples
Known GenesATP1A3, GRIK5, RABAC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567541
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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