A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044559



Internal ID19133778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115307162..115451333hg38UCSC Ensembl
Innerchr10:117066672..117210843hg19UCSC Ensembl
Innerchr10:117056662..117200833hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38144172
hg19144172
hg18144172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516251
Samples
Known GenesATRNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044559
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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