A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102436



Internal ID22011671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23917621..23917700hg38UCSC Ensembl
chrX:23935738..23935817hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649394
Samples
Known GenesCXorf58
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102436
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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