A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960584



Internal ID22735556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21174394..21174394hg38UCSC Ensembl
chr7:21214013..21214013hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960584
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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