A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6167n100



Internal ID22792254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160604003..160647923hg38UCSC Ensembl
chr6:161025035..161068955hg19UCSC Ensembl
chr6:160945025..160988945hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3843921
hg1943921
hg1843921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015803, nsv1033354, nsv1025771, nsv1021718
Samples
Known GenesLPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6167n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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