A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv967n100



Internal ID20152583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103975777..104014012hg38UCSC Ensembl
chr10:105735535..105773770hg19UCSC Ensembl
chr10:105725525..105763760hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3838236
hg1938236
hg1838236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046247, nsv1052171, nsv1043516
Samples
Known GenesSLK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv967n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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