A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458652



Internal ID22516535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80214998..80215110hg38UCSC Ensembl
chrX:79470497..79470609hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458652
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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