A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747371



Internal ID16041327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47600564..47685063hg38UCSC Ensembl
Innerchr10:47290567..47375083hg19UCSC Ensembl
Innerchr10:46710573..46795089hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3884500
hg1984517
hg1884517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550728
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)nssv747371
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