A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460599



Internal ID22518482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56339902..56356931hg38UCSC Ensembl
chrX:56366335..56383364hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3817030
hg1917030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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