A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058172



Internal ID19147391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31536509..31572390hg38UCSC Ensembl
Innerchr19:32027415..32063296hg19UCSC Ensembl
Innerchr19:36719255..36755136hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3835882
hg1935882
hg1835882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566572
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058172
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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