A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6198n100



Internal ID19016566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167281723..167382413hg38UCSC Ensembl
chr6:167695211..167795901hg19UCSC Ensembl
chr6:167615201..167715891hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38100691
hg19100691
hg18100691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027083, nsv1028698, nsv1016801, nsv1024007, nsv1035070, nsv1027490
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)dgv6198n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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