A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181648



Internal ID21320444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38078026..38078357hg38UCSC Ensembl
chr11:38099576..38099907hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941055
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181648
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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