A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112610



Internal ID22021843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45155063..45155197hg38UCSC Ensembl
chrX:45014308..45014442hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646295
Samples
Known GenesCXorf36
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112610
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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