A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618476



Internal ID20991547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161037716..161039433hg38UCSC Ensembl
chr6:161458748..161460465hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381718
hg191718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139904
Samples
Known GenesMAP3K4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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