A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441115



Internal ID22498985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15608728..15608728hg38UCSC Ensembl
chrX:15626851..15626851hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965594
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441115
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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