A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516404



Internal ID22574367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56447954..56478575hg38UCSC Ensembl
chrX:56474387..56505008hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3830622
hg1930622
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973323
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516404
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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