A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058414



Internal ID18800945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27705300..28211201hg38UCSC Ensembl
Innerchr19:28196208..28702108hg19UCSC Ensembl
Innerchr19:32888048..33393948hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38505902
hg19505901
hg18505901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724338
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)nsv1058414
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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