A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2673n100



Internal ID20154289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101182262..101351332hg38UCSC Ensembl
chr15:101722467..101891537hg19UCSC Ensembl
chr15:99539990..99709060hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38169071
hg19169071
hg18169071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044337, nsv1040181
Samples
Known GenesCHSY1, LOC100507472, PCSK6, SNRPA1, VIMP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2673n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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