A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969129



Internal ID22744064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48244913..48447745hg38UCSC Ensembl
chrX:48104348..48306117hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38202833
hg19201770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460997
Samples
Known GenesSSX1, SSX3, SSX4, SSX4B, SSX9
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969129
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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