A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048487



Internal ID18791018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77932810..77961559hg38UCSC Ensembl
Innerchr10:79692568..79721317hg19UCSC Ensembl
Innerchr10:79362574..79391323hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3828750
hg1928750
hg1828750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518613, nssv3522136
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)nsv1048487
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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