A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412634



Internal ID22470504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139315011..139315011hg38UCSC Ensembl
chr4:140236165..140236165hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958650
Supporting Variants
Samples
Known GenesNAA15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412634
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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