A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366197



Internal ID21023750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2838060..2843183hg38UCSC Ensembl
chr4:2839787..2844910hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg385124
hg195124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116520
Samples
Known GenesSH3BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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