A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066314



Internal ID18808845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27590120..27874168hg38UCSC Ensembl
Innerchr19:28081028..28365076hg19UCSC Ensembl
Innerchr19:32772868..33056916hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38284049
hg19284049
hg18284049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566485
Samples
Known GenesLINC00662
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066314
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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