A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516123



Internal ID22574085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30315066..30329983hg38UCSC Ensembl
chrX:30333183..30348100hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3814918
hg1914918
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977003
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516123
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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