A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439400



Internal ID22497270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2972459..2972459hg38UCSC Ensembl
chr7:3012093..3012093hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964789
Supporting Variants
Samples
Known GenesCARD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439400
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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