A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107748



Internal ID22016981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141012592..141244559hg38UCSC Ensembl
chrX:140106768..140338687hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38231968
hg19231920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644028
Samples
Known GenesLDOC1, SPANXC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107748
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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