A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549796



Internal ID15990519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1623016..1705729hg38UCSC Ensembl
Innerchr10:1665211..1747923hg19UCSC Ensembl
Innerchr10:1655211..1737923hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3882714
hg1982713
hg1882713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740230
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549796
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