A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455490



Internal ID22513367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:82998845..82998845hg38UCSC Ensembl
chrX:82253853..82253853hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455490
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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