A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456981



Internal ID22514862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4630838..4632083hg38UCSC Ensembl
chrX:4548879..4550124hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456981
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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