A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390728



Internal ID21048281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53410499..53411905hg38UCSC Ensembl
chr4:54276666..54278072hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381407
hg191407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117409
Samples
Known GenesFIP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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