A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15188601



Internal ID21327433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61273528..61273528hg38UCSC Ensembl
chr20:59848584..59848584hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936440
Supporting Variants
SamplesHG002
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15188601
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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