A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638738



Internal ID21830785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40557277..40557352hg38UCSC Ensembl
chrX:40416529..40416604hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638738
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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