A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638181



Internal ID21830228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103659721..103659791hg38UCSC Ensembl
chrX:102914649..102914719hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638181
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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