A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026668



Internal ID19115886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:56357894..56368070hg38UCSC Ensembl
Innerchr5:55653721..55663897hg19UCSC Ensembl
Innerchr5:55689478..55699654hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3810177
hg1910177
hg1810177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5670n100
Supporting Variantsnssv3642140
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)nsv1026668
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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