A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5709574



Internal ID21735895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34979935..34979935hg38UCSC Ensembl
chr15:35272136..35272136hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17196753
Samples
Known GenesZNF770
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)nsv5709574
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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