A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606650



Internal ID21554955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156369188..156369188hg38UCSC Ensembl
chr2:157225700..157225700hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109388
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606650
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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