A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462400



Internal ID22520285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9811259..9811968hg38UCSC Ensembl
chrX:9779299..9780008hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874305
Supporting Variants
Samples
Known GenesSHROOM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462400
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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