A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549799



Internal ID15990522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2289231..2812505hg38UCSC Ensembl
Innerchr10:2331425..2854697hg19UCSC Ensembl
Innerchr10:2321425..2844697hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38523275
hg19523273
hg18523273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740233
Samples
Known GenesLINC00701
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549799
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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