A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515578



Internal ID22573540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1433585..1446976hg38UCSC Ensembl
chrX:1552478..1565869hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3813392
hg1913392
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967828
Supporting Variants
Samples
Known GenesASMTL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515578
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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