A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1377n54



Internal ID22769272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105330171..105562272hg38UCSC Ensembl
chr10:107089929..107322030hg19UCSC Ensembl
chr10:107079919..107312020hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38232102
hg19232102
hg18232102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552094, nsv552091, nsv552093, nsv552096, nsv552092, nsv552095
Samples1780862414_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1377n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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