A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388977



Internal ID22446847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28160503..28160503hg38UCSC Ensembl
chr16:28171824..28171824hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969566
Supporting Variants
Samples
Known GenesXPO6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388977
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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