A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104193



Internal ID22013426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21728206..21728263hg38UCSC Ensembl
chrX:21746324..21746381hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640182
Samples
Known GenesSMPX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104193
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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