A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067530



Internal ID18810061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29962435..30013166hg38UCSC Ensembl
Innerchr19:30453342..30504073hg19UCSC Ensembl
Innerchr19:35145182..35195913hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3850732
hg1950732
hg1850732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3510n100
Supporting Variantsnssv3566537, nssv3566536
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)nsv1067530
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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