A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464668



Internal ID22522556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44801909..44801909hg38UCSC Ensembl
chrX:44661155..44661155hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962369
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464668
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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