A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646069



Internal ID21838116
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 StatusS
Merged Variantsnsv6101151
Supporting Variants
Samples
Known GenesZNF41
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646069
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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