A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261684



Internal ID20828724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98812958..98813579hg38UCSC Ensembl
chr2:99429421..99430042hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547498
Supporting Variants
Samples
Known GenesKIAA1211L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261684
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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