A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571995



Internal ID18870276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27550910hg38UCSC Ensembl
Innerchr19:27747981..28041818hg19UCSC Ensembl
Innerchr19:32439821..32733658hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38293838
hg19293838
hg18293838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065696
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3571995
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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