A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436956



Internal ID22494826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130128301..130128879hg38UCSC Ensembl
chrX:129262276..129262854hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879284
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436956
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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