A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554004



Internal ID327200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68629841..68657580hg38UCSC Ensembl
chrX:67849683..67877422hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3827740
hg1927740
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740544
Samples
Known GenesSTARD8
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554004
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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