A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389929



Internal ID21047482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38615804..38623565hg38UCSC Ensembl
chr4:38617425..38625186hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387762
hg197762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116023
Samples
Known GenesFLJ13197
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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