A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655430



Internal ID18607025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167267069..167361462hg38UCSC Ensembl
Innerchr6:167680557..167774950hg19UCSC Ensembl
Innerchr6:167600547..167694940hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3894394
hg1994394
hg1894394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026070
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)nssv3655430
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer