A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109000



Internal ID22018233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102556193..102562334hg38UCSC Ensembl
chrX:101811121..101817262hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg386142
hg196142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639002
Samples
Known GenesNXF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109000
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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