A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055725



Internal ID18798256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35364439..35385961hg38UCSC Ensembl
Innerchr19:35855341..35876863hg19UCSC Ensembl
Innerchr19:40547181..40568703hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3821523
hg1921523
hg1821523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n100
Supporting Variantsnssv3568160
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)nsv1055725
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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