A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465768



Internal ID22523657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65121142..65160241hg38UCSC Ensembl
chrX:64341022..64380121hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3839100
hg1939100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465768
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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