A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268379



Internal ID20477597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2844491..2844571hg38UCSC Ensembl
chrX:2762532..2762612hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764708
Supporting Variants
Samples
Known GenesGYG2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268379
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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