A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6177n100



Internal ID20157793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162188687..162466513hg38UCSC Ensembl
chr6:162609719..162887545hg19UCSC Ensembl
chr6:162529709..162807535hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38277827
hg19277827
hg18277827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025841, nsv1025236
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)dgv6177n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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