A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360605



Internal ID21018158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87269936..87270965hg38UCSC Ensembl
chr3:87319086..87320115hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg381030
hg191030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104180
Samples
Known GenesPOU1F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360605
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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