A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038636



Internal ID93501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79556772..79614541hg38UCSC Ensembl
chr10:81316528..81374297hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3857770
hg1957770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561587
Supporting Variants
Samples
Known GenesSFTPA1, SFTPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038636
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.266084


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