A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516246



Internal ID22574208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42712279..42717640hg38UCSC Ensembl
chrX:42571530..42576891hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg385362
hg195362
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971002
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516246
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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