A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17235062



Internal ID21682571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15295062..15295062hg38UCSC Ensembl
chrX:15313184..15313184hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5727813
Supporting Variants
Samples
Known GenesASB11
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17235062
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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