A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467655



Internal ID22525547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30789717..30795320hg38UCSC Ensembl
chrX:30807834..30813437hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg385604
hg195604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467655
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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