A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903710



Internal ID22678879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77961607..78271368hg38UCSC Ensembl
chr4:78882761..79192522hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38309762
hg19309762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419820
Samples
Known GenesFRAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903710
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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