A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635980



Internal ID18934261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28936088..29147730hg38UCSC Ensembl
Innerchr5:28936195..29147837hg19UCSC Ensembl
Innerchr5:28971952..29183594hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38211643
hg19211643
hg18211643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027037
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)nssv3635980
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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