A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6085n100



Internal ID22792172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87443361..87700332hg38UCSC Ensembl
chr6:88153079..88410050hg19UCSC Ensembl
chr6:88209798..88466769hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38256972
hg19256972
hg18256972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031460, nsv1026482, nsv1027706
Samples
Known GenesAKIRIN2, C6orf165, ORC3, RARS2, SLC35A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6085n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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