A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6077n100



Internal ID22792164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82010915..82027739hg38UCSC Ensembl
chr6:82720632..82737456hg19UCSC Ensembl
chr6:82777351..82794175hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3816825
hg1916825
hg1816825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021793, nsv1020964
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)dgv6077n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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