A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104481



Internal ID22013714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142829825..142829969hg38UCSC Ensembl
chrX:141917611..141917755hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104481
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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