A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181747



Internal ID21320543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1804125..1804257hg38UCSC Ensembl
chr11:1825355..1825487hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948700
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181747
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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