A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640707



Internal ID21589012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63727735..63727735hg38UCSC Ensembl
chr6:64437628..64437628hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157758
SamplesHG02818
Known GenesEYS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640707
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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