A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111151



Internal ID22020384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54082517..54082652hg38UCSC Ensembl
chrX:54108950..54109085hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638358
Samples
Known GenesFAM120C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111151
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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