A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602419



Internal ID20975490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118929601..118938800hg38UCSC Ensembl
chr6:119250766..119259965hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214555
Samples
Known GenesMCM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602419
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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