A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101151



Internal ID22010384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47472839..47472918hg38UCSC Ensembl
chrX:47332238..47332317hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646069
Samples
Known GenesZNF41
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101151
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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