A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469381



Internal ID22527271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48674163..48674441hg38UCSC Ensembl
chrX:48532552..48532830hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469381
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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