A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462578



Internal ID22520463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2842831..2843695hg38UCSC Ensembl
chrX:2760872..2761736hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867624
Supporting Variants
Samples
Known GenesGYG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462578
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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