A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955923



Internal ID16958110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:158803521..158803572hg38UCSC Ensembl
Outerchr6:159224553..159224604hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003522
SamplesBILGI_BIOE
Known GenesEZR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955923
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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