A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437773



Internal ID22495643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149387248..149387248hg38UCSC Ensembl
chrX:148468778..148468778hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437773
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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