A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440540



Internal ID22498410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140411719..140420804hg38UCSC Ensembl
chrX:139493884..139502969hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg389086
hg199086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878482
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440540
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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