A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606786



Internal ID20979857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156018325..156026949hg38UCSC Ensembl
chr6:156339459..156348083hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg388625
hg198625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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