A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462472



Internal ID22520357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41016136..41016136hg38UCSC Ensembl
chrX:40875389..40875389hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959989
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462472
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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