A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056637



Internal ID18799168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29962116..30028098hg38UCSC Ensembl
Innerchr19:30453023..30519005hg19UCSC Ensembl
Innerchr19:35144863..35210845hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3865983
hg1965983
hg1865983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3509n100
Supporting Variantsnssv3566535
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)nsv1056637
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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