A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106304



Internal ID22015537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100231428..100251230hg38UCSC Ensembl
chrX:99486426..99506228hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3819803
hg1919803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106304
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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