A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv987n100



Internal ID22787074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122379070..122437149hg38UCSC Ensembl
chr10:124138586..124196665hg19UCSC Ensembl
chr10:124128576..124186655hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3858080
hg1958080
hg1858080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040229, nsv1050574, nsv1048754, nsv1035914, nsv1054033
Samples
Known GenesMIR3941, PLEKHA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv987n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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