A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608427



Internal ID20981498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120204420..120481525hg38UCSC Ensembl
chr6:120525566..120802671hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38277106
hg19277106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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