A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608934



Internal ID20982005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160988701..160995700hg38UCSC Ensembl
chr6:161409733..161416732hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216737
Samples
Known GenesMAP3K4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608934
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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