A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026497



Internal ID18769029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17630..63270hg38UCSC Ensembl
Innerchr5:17630..63385hg19UCSC Ensembl
Innerchr5:70630..116385hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3845641
hg1945756
hg1845756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5516n100
Supporting Variantsnssv3636547
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)nsv1026497
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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