A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465930



Internal ID22523820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68668125..68668277hg38UCSC Ensembl
chrX:67887967..67888119hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881256
Supporting Variants
Samples
Known GenesSTARD8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465930
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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