A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6135n100



Internal ID22792222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106988892..107234753hg38UCSC Ensembl
chr6:107310094..107555957hg19UCSC Ensembl
chr6:107416787..107662650hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38245862
hg19245864
hg18245864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025321, nsv1019898, nsv1020715
Samples
Known GenesBEND3, C6orf203, PDSS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6135n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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