A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436895



Internal ID22494765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103554035..103571450hg38UCSC Ensembl
chrX:102808963..102826378hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3817416
hg1917416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436895
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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