A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515965



Internal ID22573927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21338849..21343208hg38UCSC Ensembl
chrX:21356967..21361326hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg384360
hg194360
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974236
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515965
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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