A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049256



Internal ID21958491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36505345..36505345hg38UCSC Ensembl
chr2:36732488..36732488hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528819
Samples
Known GenesCRIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049256
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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