A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061287



Internal ID21970520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118005605..118005605hg38UCSC Ensembl
chr5:117341300..117341300hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554053
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061287
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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