A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655428



Internal ID18607023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167267069..167359345hg38UCSC Ensembl
Innerchr6:167680557..167772833hg19UCSC Ensembl
Innerchr6:167600547..167692823hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3892277
hg1992277
hg1892277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028156
Supporting Variants
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)nssv3655428
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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