A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256633



Internal ID20823673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119975525..119976248hg38UCSC Ensembl
chr2:120733101..120733824hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552956
Supporting Variants
Samples
Known GenesPTPN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256633
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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