A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17234007



Internal ID21681516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66811668..66811668hg38UCSC Ensembl
chr7:66276655..66276655hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5717205
Supporting Variants
Samples
Known GenesGTF2IRD1P1
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)nssv17234007
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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