A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467787



Internal ID22525679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56919021..56930413hg38UCSC Ensembl
chrX:56945454..56956846hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3811393
hg1911393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876080
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467787
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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