A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402677



Internal ID21060230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34478631..34480086hg38UCSC Ensembl
chr6:34446408..34447863hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381456
hg191456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232849
Samples
Known GenesPACSIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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