A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435092



Internal ID22492962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150977290..150977341hg38UCSC Ensembl
chrX:150145763..150145814hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435092
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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