A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv962n100



Internal ID22787049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95105324..95125577hg38UCSC Ensembl
chr10:96865081..96885334hg19UCSC Ensembl
chr10:96855071..96875324hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3820254
hg1920254
hg1820254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041130, nsv1046150, nsv1042421
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv962n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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