A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000632



Internal ID16946898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6055404..6055909hg38UCSC Ensembl
Outerchr10:6097367..6097872hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956342
Supporting Variants
SamplesBILGI_BIOE
Known GenesIL2RA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000632
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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