A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256118



Internal ID20823158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173165419..173165935hg38UCSC Ensembl
chr2:174030147..174030663hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535855
Supporting Variants
Samples
Known GenesZAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256118
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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