A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176550



Internal ID21315346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71855998..71856325hg38UCSC Ensembl
chr17:69852139..69852466hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927482
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176550
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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