A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459235



Internal ID22517118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85087981..85088213hg38UCSC Ensembl
chrX:84342987..84343219hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876470
Supporting Variants
Samples
Known GenesAPOOL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459235
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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