A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076951



Internal ID21986184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62371563..62371563hg38UCSC Ensembl
chr5:61667390..61667390hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541008
Samples
Known GenesKIF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076951
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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