A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450195



Internal ID22508065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44520541..44522099hg38UCSC Ensembl
chrX:44379787..44381345hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381559
hg191559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450195
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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