A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015334



Internal ID20582374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94155817..94156359hg38UCSC Ensembl
chr13:94808071..94808613hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480191
Supporting Variants
Samples
Known GenesGPC6, GPC6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015334
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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