A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6150n100



Internal ID22792237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136846782..136915639hg38UCSC Ensembl
chr6:137167920..137236777hg19UCSC Ensembl
chr6:137209613..137278470hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3868858
hg1968858
hg1868858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025170, nsv1024719
Samples
Known GenesPEX7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6150n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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