A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv758785



Internal ID16052741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115464095..115565511hg38UCSC Ensembl
Innerchr10:117223605..117325021hg19UCSC Ensembl
Innerchr10:117213595..117315011hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38101417
hg19101417
hg18101417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552204
Supporting Variants
Samples
Known GenesATRNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv758785
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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