A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071675



Internal ID21463229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79542902..80213948hg38UCSC Ensembl
chr10:81302658..81973704hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38671047
hg19671047
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672415
Supporting Variants
SamplesHG03009
Known GenesANXA11, BEND3P3, LINC00857, LOC100288974, LOC642361, MBL1P, NUTM2B, PLAC9, SFTPA1, SFTPA2, SFTPD, TMEM254, TMEM254-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071675
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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