A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107872



Internal ID22017107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55749349..55749403hg38UCSC Ensembl
chrX:55775782..55775836hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637869
Samples
Known GenesRRAGB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107872
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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