A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401573



Internal ID21059126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139771627..139774743hg38UCSC Ensembl
chr5:139151212..139154328hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg383117
hg193117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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