A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516102



Internal ID22574064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2886627..2900077hg38UCSC Ensembl
chrX:2804668..2818118hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3813451
hg1913451
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516102
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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