A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17205592



Internal ID21653101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110348163..110348163hg38UCSC Ensembl
chrX:109591391..109591391hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5724086
Supporting Variants
Samples
Known GenesAMMECR1
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17205592
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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