A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015796



Internal ID18758330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28956203..29375048hg38UCSC Ensembl
Innerchr6:28923980..29342825hg19UCSC Ensembl
Innerchr6:29031959..29450804hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38418846
hg19418846
hg18418846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745363
Samples
Known GenesLOC100129636, OR12D3, OR14J1, OR2B3, OR2J2, OR2J3, OR2W1, OR5V1, ZNF311
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015796
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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