A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108946



Internal ID22018179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48960238..48960326hg38UCSC Ensembl
chrX:48817499..48817587hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108946
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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