A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647062



Internal ID21839109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47105351..47105406hg38UCSC Ensembl
chrX:46964750..46964805hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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