A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555743



Internal ID328893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27013073..27013703hg38UCSC Ensembl
chrX:27031190..27031820hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555743
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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