A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399599



Internal ID21057152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25130073..25137329hg38UCSC Ensembl
chr6:25130301..25137557hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387257
hg197257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140679
Samples
Known GenesCMAHP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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