A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515631



Internal ID22573593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151558815..151565593hg38UCSC Ensembl
chrX:150727287..150734065hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386779
hg196779
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978648
Supporting Variants
Samples
Known GenesPASD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515631
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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