A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600929



Internal ID20974000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132593330..132593869hg38UCSC Ensembl
chr6:132914469..132915008hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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