A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859652



Internal ID22043295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2822220..2822220hg38UCSC Ensembl
chr7:2861854..2861854hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6261015
Supporting Variants
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859652
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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