A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978648



Internal ID22753583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151558815..151565593hg38UCSC Ensembl
chrX:150727287..150734065hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386779
hg196779
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515631
Samples
Known GenesPASD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978648
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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