A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055678



Internal ID18798209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29965945..30019304hg38UCSC Ensembl
Innerchr19:30456852..30510211hg19UCSC Ensembl
Innerchr19:35148692..35202051hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3853360
hg1953360
hg1853360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3510n100
Supporting Variantsnssv3566555
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055678
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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