A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260896



Internal ID20827936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63941536..63941702hg38UCSC Ensembl
chr2:64168670..64168836hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545620
Supporting Variants
Samples
Known GenesVPS54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260896
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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