A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178886



Internal ID21317682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3800531..3800606hg38UCSC Ensembl
chr3:3842215..3842290hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939270
Supporting Variants
SamplesHG002
Known GenesLRRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178886
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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