A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004918



Internal ID16951184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6022812..6022871hg38UCSC Ensembl
Outerchr10:6064775..6064834hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958561
Supporting Variants
SamplesBILGI_BIOE
Known GenesIL2RA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004918
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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