A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515672



Internal ID22573634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153192206..153203851hg38UCSC Ensembl
chrX:152461535..152473192hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3811646
hg1911658
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515672
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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