A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135075



Internal ID21416800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154378944..154379263hg38UCSC Ensembl
chr3:154096733..154097052hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583610
Supporting Variants
SamplesHG00731
Known GenesGPR149
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135075
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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