A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024891



Internal ID19114108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141667329..141753178hg38UCSC Ensembl
Innerchr6:141988466..142074315hg19UCSC Ensembl
Innerchr6:142030159..142116008hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3885850
hg1985850
hg1885850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749553
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)nsv1024891
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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