A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409031



Internal ID22466901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38902085..38902085hg38UCSC Ensembl
chr19:39392725..39392725hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977088
Supporting Variants
Samples
Known GenesNFKBIB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409031
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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