A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366510



Internal ID21024063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169330601..169331600hg38UCSC Ensembl
chr3:169048389..169049388hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097462
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366510
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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