A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038634



Internal ID93499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79543104..80217086hg38UCSC Ensembl
chr10:81302860..81976842hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38673983
hg19673983
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563886
Supporting Variants
Samples
Known GenesANXA11, BEND3P3, LINC00857, LOC100288974, LOC642361, MBL1P, NUTM2B, PLAC9, SFTPA1, SFTPA2, SFTPD, TMEM254, TMEM254-AS1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038634
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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