A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458737



Internal ID22516620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22736317..22736370hg38UCSC Ensembl
chrX:22754434..22754487hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875964
Supporting Variants
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458737
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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