A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958517



Internal ID16960705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:133214065..133214183hg38UCSC Ensembl
Outerchr8:134226308..134226426hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001231
SamplesBILGI_BIOE
Known GenesWISP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958517
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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