A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084539



Internal ID21461761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94288792..94288792hg38UCSC Ensembl
chr13:94941046..94941046hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649818
Supporting Variants
SamplesHG02818
Known GenesGPC6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084539
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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