A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5958n100



Internal ID22792045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45028977..45071682hg38UCSC Ensembl
chr6:44996714..45039419hg19UCSC Ensembl
chr6:45104692..45147397hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3842706
hg1942706
hg1842706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024404, nsv1018962
Samples
Known GenesSUPT3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5958n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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