A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101111



Internal ID22010344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47148846..47148897hg38UCSC Ensembl
chrX:47008245..47008296hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639543
Samples
Known GenesRBM10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101111
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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