A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396677



Internal ID21054230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2423979..2451084hg38UCSC Ensembl
chr6:2424213..2451318hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3827106
hg1927106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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