A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029742



Internal ID18772273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:157816662..157844585hg38UCSC Ensembl
Innerchr5:157243670..157271593hg19UCSC Ensembl
Innerchr5:157176248..157204171hg18UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3827924
hg1927924
hg1827924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648223, nssv3648222
Samples
Known GenesCLINT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029742
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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