A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748926



Internal ID16042882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:62222909..62300509hg38UCSC Ensembl
Innerchr10:63982668..64060268hg19UCSC Ensembl
Innerchr10:63652674..63730274hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3877601
hg1977601
hg1877601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551181
Supporting Variants
Samples
Known GenesRTKN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv748926
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