A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061232



Internal ID18803763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15166388..15191569hg38UCSC Ensembl
Innerchr19:15277199..15302380hg19UCSC Ensembl
Innerchr19:15138199..15163380hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3825182
hg1925182
hg1825182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3439n100
Supporting Variantsnssv3564782, nssv3564783, nssv3564784
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)nsv1061232
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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