A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516251



Internal ID18814532
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 StatusS
Merged Variantsnsv1044559
Supporting Variants
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)nssv3516251
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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