A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3646939



Internal ID18945220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106781755..106805716hg38UCSC Ensembl
Innerchr5:106117456..106141417hg19UCSC Ensembl
Innerchr5:106145355..106169316hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3823962
hg1923962
hg1823962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026307
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)nssv3646939
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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