A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889909



Internal ID22664931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53406138..53406271hg38UCSC Ensembl
chr4:54272305..54272438hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427379
Samples
Known GenesFIP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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