A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028698



Internal ID18771229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167285281..167357173hg38UCSC Ensembl
Innerchr6:167698769..167770661hg19UCSC Ensembl
Innerchr6:167618759..167690651hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3871893
hg1971893
hg1871893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6198n100
Supporting Variantsnssv3655439
Samples
Known GenesTTLL2, UNC93A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028698
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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