A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7213n100



Internal ID20158829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50716059..50951075hg38UCSC Ensembl
chr8:51628619..51863635hg19UCSC Ensembl
chr8:51791172..52026188hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38235017
hg19235017
hg18235017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029698, nsv1019760
Samples
Known GenesSNTG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7213n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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