A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072031



Internal ID21981264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48675532..48675532hg38UCSC Ensembl
chr3:48712965..48712965hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549681
Samples
Known GenesNCKIPSD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072031
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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