A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111521



Internal ID22020754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53534894..53535203hg38UCSC Ensembl
chrX:53561855..53562164hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643674
Samples
Known GenesHUWE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111521
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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