A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6186n100



Internal ID20157802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162324536..162400006hg38UCSC Ensembl
chr6:162745568..162821038hg19UCSC Ensembl
chr6:162665558..162741028hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3875471
hg1975471
hg1875471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033809, nsv1022710, nsv1029857
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)dgv6186n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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