A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439871



Internal ID22497741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18852380..18854904hg38UCSC Ensembl
chrX:18870498..18873022hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg382525
hg192525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439871
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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