A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399109



Internal ID21056662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94732368..95017097hg38UCSC Ensembl
chr6:95442086..95680543hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38284730
hg19238458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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