A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026482



Internal ID18769014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:87455216..87700010hg38UCSC Ensembl
Innerchr6:88164934..88409728hg19UCSC Ensembl
Innerchr6:88221653..88466447hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38244795
hg19244795
hg18244795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6085n100
Supporting Variantsnssv3648941
Samples
Known GenesAKIRIN2, C6orf165, ORC3, RARS2, SLC35A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026482
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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