A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442308



Internal ID22500178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143986148..144002593hg38UCSC Ensembl
chrX:143069254..143085699hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3816446
hg1916446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872135
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442308
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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