A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560898



Internal ID333892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73125904..73127140hg38UCSC Ensembl
chrX:72345743..72346979hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg381237
hg191237
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740715
Samples
Known GenesNAP1L6
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560898
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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