A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058546



Internal ID18801077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3321667..3369170hg38UCSC Ensembl
Innerchr19:3321665..3369168hg19UCSC Ensembl
Innerchr19:3272665..3320168hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3847504
hg1947504
hg1847504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723253
Samples
Known GenesNFIC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058546
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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