A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379048



Internal ID22436918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1986849..1986898hg38UCSC Ensembl
chr16:2036850..2036899hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931490
Supporting Variants
Samples
Known GenesGFER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379048
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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