A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177318



Internal ID21316114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3820807..3820915hg38UCSC Ensembl
chr19:3820805..3820913hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929352
Supporting Variants
SamplesHG002
Known GenesZFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177318
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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