A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6172n100



Internal ID22792259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161925250..162180183hg38UCSC Ensembl
chr6:162346282..162601215hg19UCSC Ensembl
chr6:162266272..162521205hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38254934
hg19254934
hg18254934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020928, nsv1022804
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6172n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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