A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412837



Internal ID22470707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70867736..70867736hg38UCSC Ensembl
chr4:71733453..71733453hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951893
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412837
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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