A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399449



Internal ID21057002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41343787..41348967hg38UCSC Ensembl
chr6:41311525..41316705hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385181
hg195181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143324
Samples
Known GenesNCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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