A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366781



Internal ID21024334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136709896..136720570hg38UCSC Ensembl
chr3:136428738..136439412hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3810675
hg1910675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094955
Samples
Known GenesSTAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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