A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181638



Internal ID21320434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22637509..22637608hg38UCSC Ensembl
chr11:22659055..22659154hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941442
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181638
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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