A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067291



Internal ID19156510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8862308..8888635hg38UCSC Ensembl
Innerchr19:8972984..8999311hg19UCSC Ensembl
Innerchr19:8833984..8860311hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3826328
hg1926328
hg1826328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564682
Samples
Known GenesMUC16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067291
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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