A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569786



Internal ID18521381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19310409..19399802hg38UCSC Ensembl
Innerchr19:19421218..19510611hg19UCSC Ensembl
Innerchr19:19282218..19371611hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3889394
hg1989394
hg1889394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056419
Supporting Variants
Samples
Known GenesGATAD2A, MAU2, SUGP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569786
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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