A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023317



Internal ID19112534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..63270hg38UCSC Ensembl
Innerchr5:15520..63385hg19UCSC Ensembl
Innerchr5:68520..116385hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3847751
hg1947866
hg1847866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5511n100
Supporting Variantsnssv3636501
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)nsv1023317
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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