A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5877n100



Internal ID22791964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:249798..350608hg38UCSC Ensembl
chr6:249798..350608hg19UCSC Ensembl
chr6:194798..295608hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38100811
hg19100811
hg18100811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030110, nsv1020150, nsv1023033, nsv1034543, nsv1023821
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5877n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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