A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469619



Internal ID22527509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5782884..5784145hg38UCSC Ensembl
chrX:5700925..5702186hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg381262
hg191262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469619
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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