A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372829



Internal ID22598498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27062458..27062458hg38UCSC Ensembl
chr15:27307605..27307605hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979418
Supporting Variants
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372829
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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