A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464107



Internal ID22521993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27874027..27874449hg38UCSC Ensembl
chrX:27892144..27892566hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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