A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432187



Internal ID22490057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112530783..112536273hg38UCSC Ensembl
chrX:111774011..111779501hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385491
hg195491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868256
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432187
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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