A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605802



Internal ID20978873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137773756..137774208hg38UCSC Ensembl
chr6:138094893..138095345hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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