A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516624



Internal ID22574587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66710684..66742175hg38UCSC Ensembl
chrX:65930526..65962017hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3831492
hg1931492
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975970
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516624
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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