A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602734



Internal ID20975805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139504976..139511979hg38UCSC Ensembl
chr6:139826113..139833116hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg387004
hg197004
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602734
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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