A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017981



Internal ID18760514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167267069..167351763hg38UCSC Ensembl
Innerchr6:167680557..167765251hg19UCSC Ensembl
Innerchr6:167600547..167685241hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3884695
hg1984695
hg1884695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6197n100
Supporting Variantsnssv3655419
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)nsv1017981
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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