A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262117



Internal ID20471335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118278338..118278502hg38UCSC Ensembl
chrX:117412301..117412465hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262117
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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