A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15175860



Internal ID21314656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51479173..51479229hg38UCSC Ensembl
chr16:51513084..51513140hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936528
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15175860
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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