A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176128



Internal ID21314924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69325359..69325427hg38UCSC Ensembl
chr16:69359262..69359330hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954259
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176128
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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