A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280672



Internal ID20489890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136949107..136949235hg38UCSC Ensembl
chrX:136031266..136031394hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767419
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280672
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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