A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059341



Internal ID18801872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15173926..15186765hg38UCSC Ensembl
Innerchr19:15284737..15297576hg19UCSC Ensembl
Innerchr19:15145737..15158576hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3812840
hg1912840
hg1812840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3440n100
Supporting Variantsnssv3723291
Samples
Known GenesMIR6795, NOTCH3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059341
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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