A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6112n100



Internal ID20157728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99829964..100202622hg38UCSC Ensembl
chr6:100277840..100650498hg19UCSC Ensembl
chr6:100384561..100757219hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38372659
hg19372659
hg18372659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019210, nsv1032075, nsv1023038
Samples
Known GenesMCHR2, MCHR2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6112n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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