A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739057



Internal ID162723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6309585..6309651hg38UCSC Ensembl
chrX:6227626..6227692hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739057
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer