A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002287



Internal ID18845701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1495604..1496905hg38UCSC Ensembl
Outerchr10:1537799..1539100hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153632
Supporting Variants
SamplesKWB1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002287
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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