A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6164n100



Internal ID22792251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153640752..153712427hg38UCSC Ensembl
chr6:153961887..154033562hg19UCSC Ensembl
chr6:154003580..154075255hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3871676
hg1971676
hg1871676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024992, nsv1027141
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6164n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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