A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137595



Internal ID21446766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183017819..183017819hg38UCSC Ensembl
chr3:182735607..182735607hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608599
Supporting Variants
SamplesHG00732
Known GenesMCCC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137595
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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