A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454778



Internal ID22512655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38466093..38466144hg38UCSC Ensembl
chrX:38325346..38325397hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454778
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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