A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361261



Internal ID21018814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44767668..44786019hg38UCSC Ensembl
chr3:44809160..44827511hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3818352
hg1918352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100619
Samples
Known GenesKIF15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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