A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1266n54



Internal ID18993442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74477740..74614146hg38UCSC Ensembl
chr10:76237498..76373904hg19UCSC Ensembl
chr10:75907504..76043910hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38136407
hg19136407
hg18136407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551532, nsv551534, nsv551533
SamplesNINDS_147, NINDS_145
Known GenesADK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1266n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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