A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381419



Internal ID21038972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54390381..54664457hg38UCSC Ensembl
chr4:55256548..55530623hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38274077
hg19274076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117465
Samples
Known GenesKIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381419
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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