A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067099



Internal ID18809630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29964373..30020645hg38UCSC Ensembl
Innerchr19:30455280..30511552hg19UCSC Ensembl
Innerchr19:35147120..35203392hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3856273
hg1956273
hg1856273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3510n100
Supporting Variantsnssv3566552, nssv3566551
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)nsv1067099
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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