A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466676



Internal ID22524568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71640916..71642355hg38UCSC Ensembl
chrX:70860766..70862205hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg381440
hg191440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880893
Supporting Variants
Samples
Known GenesBCYRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466676
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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