A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103822



Internal ID22013055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107152058..107152126hg38UCSC Ensembl
chrX:106395288..106395356hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646224
Samples
Known GenesNUP62CL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103822
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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