A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450913



Internal ID22508786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74184674..74184674hg38UCSC Ensembl
chrX:73404509..73404509hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954739
Supporting Variants
Samples
Known GenesFTX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450913
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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