A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529021



Internal ID15109628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:132682477..132750285hg38UCSC Ensembl
Innerchr5:132018169..132085977hg19UCSC Ensembl
Innerchr5:132046068..132113876hg18UCSC Ensembl
Innerchr5:132046068..132113876hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3867809
hg1967809
hg1867809
hg1767809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705732
Samples
Known GenesCCNI2, IL4, KIF3A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529021
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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