A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419700



Internal ID22477570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37014997..37014997hg38UCSC Ensembl
chr4:37016619..37016619hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419700
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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