A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029024



Internal ID19118243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:82380709..82426019hg38UCSC Ensembl
Innerchr5:81676528..81721838hg19UCSC Ensembl
Innerchr5:81712284..81757594hg18UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3845311
hg1945311
hg1845311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639138
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)nsv1029024
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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