A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181118



Internal ID21319914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20981520..20981617hg38UCSC Ensembl
chr1:21308013..21308110hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940052
Supporting Variants
SamplesHG002
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181118
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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