A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516210



Internal ID22574172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3815363..3824731hg38UCSC Ensembl
chrX:3733404..3742772hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg389369
hg199369
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972086
Supporting Variants
Samples
Known GenesLOC389906
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516210
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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