A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630877



Internal ID21579182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39346135..39346135hg38UCSC Ensembl
chr6:39313911..39313911hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151026
SamplesNA19650
Known GenesKIF6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630877
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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