A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031882



Internal ID19121104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167211842..167382413hg38UCSC Ensembl
Innerchr6:167625330..167795901hg19UCSC Ensembl
Innerchr6:167545320..167715891hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38170572
hg19170572
hg18170572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6196n100
Supporting Variantsnssv3655417
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)nsv1031882
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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