A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026644



Internal ID18769176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..137002hg38UCSC Ensembl
Innerchr5:15520..137117hg19UCSC Ensembl
Innerchr5:68520..190117hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38121483
hg19121598
hg18121598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5514n100
Supporting Variantsnssv3636531, nssv3636530
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)nsv1026644
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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