A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461750



Internal ID22519635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84354882..84354945hg38UCSC Ensembl
chrX:83609890..83609953hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874330
Supporting Variants
Samples
Known GenesHDX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461750
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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