A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070431



Internal ID21979664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44390924..44390924hg38UCSC Ensembl
chr6:44358661..44358661hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569137
Samples
Known GenesCDC5L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070431
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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