A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024007



Internal ID18766540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167285281..167370566hg38UCSC Ensembl
Innerchr6:167698769..167784054hg19UCSC Ensembl
Innerchr6:167618759..167704044hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3885286
hg1985286
hg1885286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6198n100
Supporting Variantsnssv3655440
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)nsv1024007
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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