A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183583



Internal ID21322380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93454323..93454478hg38UCSC Ensembl
chr13:94106576..94106731hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3955164
Supporting Variants
SamplesHG002
Known GenesGPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183583
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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