A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609575



Internal ID20982646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109914478..109972426hg38UCSC Ensembl
chr6:110235681..110293629hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3857949
hg1957949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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