A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027513



Internal ID18770045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167267069..167382413hg38UCSC Ensembl
Innerchr6:167680557..167795901hg19UCSC Ensembl
Innerchr6:167600547..167715891hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38115345
hg19115345
hg18115345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6197n100
Supporting Variantsnssv3655431
Samples
Known GenesTCP10, TTLL2, UNC93A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027513
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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