A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073955



Internal ID21983188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1446237..1446237hg38UCSC Ensembl
chr7:1485873..1485873hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574938
Samples
Known GenesMICALL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073955
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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