A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181082



Internal ID21319878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18597958..18598028hg38UCSC Ensembl
chr1:18924452..18924522hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954602
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181082
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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