A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461467



Internal ID22519351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45521142..45522192hg38UCSC Ensembl
chrX:45380387..45381437hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381051
hg191051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878144
Supporting Variants
Samples
Known GenesLOC101927528
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461467
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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