A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460659



Internal ID22518542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56869574..56871093hg38UCSC Ensembl
chrX:56896007..56897526hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg381520
hg191520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460659
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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