A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390461



Internal ID21048014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41045482..41074799hg38UCSC Ensembl
chr4:41047499..41076816hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3829318
hg1929318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116344
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390461
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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