A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381409



Internal ID21038962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47676689..47684359hg38UCSC Ensembl
chr4:47678706..47686376hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg387671
hg197671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117236
Samples
Known GenesCORIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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