A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv963n100



Internal ID19011331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97031342..97113892hg38UCSC Ensembl
chr10:98791099..98873649hg19UCSC Ensembl
chr10:98781089..98863639hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3882551
hg1982551
hg1882551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040262, nsv1039568, nsv1037576
Samples
Known GenesLOC100505540, SLIT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv963n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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