A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6192n100



Internal ID20157808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162537326..162619009hg38UCSC Ensembl
chr6:162958358..163040041hg19UCSC Ensembl
chr6:162878348..162960031hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3881684
hg1981684
hg1881684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034971, nsv1031355
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)dgv6192n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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