A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397036



Internal ID21054589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9811101..9812900hg38UCSC Ensembl
chr6:9811334..9813133hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397036
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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