A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554627



Internal ID327806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6731833..6744638hg38UCSC Ensembl
chrX:6649874..6662679hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3812806
hg1912806
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554627
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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