A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028156



Internal ID18770687
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 StatusM
Merged Variantsdgv6197n100
Supporting Variantsnssv3655422, nssv3655423, nssv3655420, nssv3655427, nssv3655426, nssv3655425, nssv3655428, nssv3655421, nssv3655429, nssv3655424
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)nsv1028156
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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