A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645730



Internal ID21837777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50795101..50795160hg38UCSC Ensembl
chrX:50538101..50538160hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107475
Supporting Variants
Samples
Known GenesSHROOM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645730
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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