A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15182436



Internal ID21321232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95196582..95196686hg38UCSC Ensembl
chr13:95848836..95848940hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927033
Supporting Variants
SamplesHG002
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15182436
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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