A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438093



Internal ID22495963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16454054..16461126hg38UCSC Ensembl
chrX:16472177..16479249hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg387073
hg197073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438093
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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