A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402297



Internal ID21059850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48698501..48721300hg38UCSC Ensembl
chr6:48666243..48688937hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3822800
hg1922695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402297
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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