A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178917



Internal ID21317713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15868481..15868547hg38UCSC Ensembl
chr3:15909988..15910054hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929719
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178917
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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