A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102049



Internal ID22011282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8169906..8467414hg38UCSC Ensembl
chrX:8137947..8435455hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38297509
hg19297509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642966
Samples
Known GenesVCX2, VCX3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102049
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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