A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604012



Internal ID20977083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129525101..129570100hg38UCSC Ensembl
chr6:129846246..129891245hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3845000
hg1945000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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