A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107576



Internal ID22016809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17425521..17425576hg38UCSC Ensembl
chrX:17443644..17443699hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639053
Samples
Known GenesNHS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107576
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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