A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760307



Internal ID16054263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121676732..121702140hg38UCSC Ensembl
Innerchr10:123436246..123461654hg19UCSC Ensembl
Innerchr10:123426236..123451644hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3825409
hg1925409
hg1825409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552240
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760307
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