A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv947n100



Internal ID20152563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86460173..86585847hg38UCSC Ensembl
chr10:88219930..88345604hg19UCSC Ensembl
chr10:88209910..88335584hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38125675
hg19125675
hg18125675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042955, nsv1045699
Samples
Known GenesWAPAL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv947n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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