A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515947



Internal ID22573909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19139111..19150027hg38UCSC Ensembl
chrX:19157229..19168145hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3810917
hg1910917
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515947
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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