A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516506



Internal ID22574469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63254636..63266858hg38UCSC Ensembl
chrX:62474513..62486735hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3812223
hg1912223
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975811
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516506
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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