A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025874



Internal ID19115091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:104174067..104199787hg38UCSC Ensembl
Innerchr5:103509768..103535488hg19UCSC Ensembl
Innerchr5:103537667..103563387hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3825721
hg1925721
hg1825721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5753n100
Supporting Variantsnssv3746469, nssv3746467, nssv3645962, nssv3746468, nssv3645959, nssv3645960, nssv3645966, nssv3645965, nssv3645963, nssv3645961, nssv3645964
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)nsv1025874
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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