A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038658



Internal ID93516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79796368..80226368hg38UCSC Ensembl
chr10:81556124..81986124hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38430001
hg19430001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483974
Supporting Variants
Samples
Known GenesANXA11, LINC00857, LOC100288974, LOC642361, MBL1P, PLAC9, SFTPD, TMEM254, TMEM254-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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