A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026307



Internal ID19115524
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 StatusM
Merged Variantsdgv5772n100
Supporting Variantsnssv3646939
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)nsv1026307
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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