A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701800



Internal ID21223626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133214071..133214071hg38UCSC Ensembl
chr8:134226314..134226314hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817589
Supporting Variants
Samples
Known GenesWISP1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701800
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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