A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458877



Internal ID22516759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27188379..27190136hg38UCSC Ensembl
chrX:27206496..27208253hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458877
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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