A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255892



Internal ID20822932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135628702..135629228hg38UCSC Ensembl
chr2:136386272..136386798hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550604
Supporting Variants
Samples
Known GenesR3HDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255892
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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