A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601079



Internal ID20974150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126500301..126503500hg38UCSC Ensembl
chr6:126821447..126824646hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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