A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181909



Internal ID21320705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31176905..31177032hg38UCSC Ensembl
chr1:31649752..31649879hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937345
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181909
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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