A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439267



Internal ID21096820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30370767..30462513hg38UCSC Ensembl
chr10:30659696..30751442hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3891747
hg1991747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188707
Samples
Known GenesMAP3K8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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