A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407607



Internal ID21065160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26575566..26577101hg38UCSC Ensembl
chr6:26575794..26577329hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381536
hg191536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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