A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515179



Internal ID22573138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116796048..116832297hg38UCSC Ensembl
chrX:115930016..115966265hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3836250
hg1936250
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971325
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515179
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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