A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110542



Internal ID22019775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9836973..9837068hg38UCSC Ensembl
chrX:9805013..9805108hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638423
Samples
Known GenesSHROOM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110542
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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