A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv925n100



Internal ID19011293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74437611..74492107hg38UCSC Ensembl
chr10:76197369..76251865hg19UCSC Ensembl
chr10:75867375..75921871hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3854497
hg1954497
hg1854497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045740, nsv1053624
Samples
Known GenesADK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv925n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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