A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029475



Internal ID19118694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:104171056..104196394hg38UCSC Ensembl
Innerchr5:103506757..103532095hg19UCSC Ensembl
Innerchr5:103534656..103559994hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3825339
hg1925339
hg1825339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5753n100
Supporting Variantsnssv3748317
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)nsv1029475
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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