A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516605



Internal ID22574568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64837698..64862791hg38UCSC Ensembl
chrX:64057578..64082671hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3825094
hg1925094
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967958
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516605
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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