A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442577



Internal ID22500447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138172678..138333241hg38UCSC Ensembl
chrX:137254837..137415400hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38160564
hg19160564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883023
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442577
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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