A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178086



Internal ID21316882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32739555..32740227hg38UCSC Ensembl
chr20:31327362..31328034hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3952685
Supporting Variants
SamplesHG002
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178086
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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