A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025272



Internal ID19114490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68341054..68385502hg38UCSC Ensembl
Innerchr6:69050946..69095394hg19UCSC Ensembl
Innerchr6:69107667..69152115hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3844449
hg1944449
hg1844449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658796
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)nsv1025272
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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