A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031396



Internal ID18773930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:63270..115984hg38UCSC Ensembl
Innerchr5:63385..116099hg19UCSC Ensembl
Innerchr5:116385..169099hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3852715
hg1952715
hg1852715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5518n100
Supporting Variantsnssv3633206, nssv3633207
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)nsv1031396
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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