A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103906



Internal ID22013139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113931159..113931222hg38UCSC Ensembl
chrX:113174435..113174506hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3864
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103906
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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