A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057728



Internal ID21966961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212763623..212763623hg38UCSC Ensembl
chr2:213628347..213628347hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057728
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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