A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469205



Internal ID22527096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35305413..35305986hg38UCSC Ensembl
chrX:35323530..35324103hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868670
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469205
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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