A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6169n100



Internal ID20157785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161644335..161956796hg38UCSC Ensembl
chr6:162065367..162377828hg19UCSC Ensembl
chr6:161985357..162297818hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38312462
hg19312462
hg18312462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030927, nsv1017412
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)dgv6169n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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