A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032468



Internal ID18775002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29001153..29187972hg38UCSC Ensembl
Innerchr6:28968930..29155749hg19UCSC Ensembl
Innerchr6:29076909..29263728hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38186820
hg19186820
hg18186820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655765
Samples
Known GenesLOC100129636, OR2B3, OR2J2, OR2J3, OR2W1, ZNF311
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032468
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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