A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575760



Internal ID20948831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79538320..80221775hg38UCSC Ensembl
chr10:81298076..81981531hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38683456
hg19683456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv819n223
Supporting Variantsnssv18231262
Samples
Known GenesANXA11, BEND3P3, LINC00857, LOC100288974, LOC642361, MBL1P, NUTM2B, PLAC9, SFTPA1, SFTPA2, SFTPD, TMEM254, TMEM254-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575760
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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