A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607411



Internal ID20980482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147980754..147981004hg38UCSC Ensembl
chr6:148301890..148302140hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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