A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103761



Internal ID22012994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26570668..27316839hg38UCSC Ensembl
chr10:26859597..27605768hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38746172
hg19746172
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593141
Samples
Known GenesABI1, ACBD5, ANKRD26, LINC00202-1, LINC00202-2, LINC00264, LRRC37A6P, MASTL, PDSS1, YME1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103761
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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