A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv758791



Internal ID16052747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115724951..115776738hg38UCSC Ensembl
Innerchr10:117484461..117536249hg19UCSC Ensembl
Innerchr10:117474451..117526239hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3851788
hg1951789
hg1851789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552210
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)nssv758791
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer