A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407029



Internal ID21064582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95782101..95783100hg38UCSC Ensembl
chr6:96229977..96230976hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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