A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748117



Internal ID16042073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52764898..52772139hg38UCSC Ensembl
Innerchr10:54524658..54531899hg19UCSC Ensembl
Innerchr10:54194664..54201905hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg387242
hg197242
hg187242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550902
Supporting Variants
Samples
Known GenesMBL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv748117
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