A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066847



Internal ID21976080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57031156..57031156hg38UCSC Ensembl
chr5:56326983..56326983hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066847
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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