A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104012



Internal ID22013245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47173895..47173954hg38UCSC Ensembl
chrX:47033294..47033353hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638070
Samples
Known GenesRBM10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104012
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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