A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6185n100



Internal ID20157801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162300763..162474720hg38UCSC Ensembl
chr6:162721795..162895752hg19UCSC Ensembl
chr6:162641785..162815742hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38173958
hg19173958
hg18173958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019778, nsv1025242, nsv1016161
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)dgv6185n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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