A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017025



Internal ID19106242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:76630453..76650440hg38UCSC Ensembl
Innerchr5:75926278..75946265hg19UCSC Ensembl
Innerchr5:75962034..75982021hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3819988
hg1919988
hg1819988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639023
Samples
Known GenesIQGAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017025
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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