A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890160



Internal ID22665186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186455504..188157234hg38UCSC Ensembl
chr4:187376658..189078388hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381701731
hg191701731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414788
Samples
Known GenesF11-AS1, FAT1, LOC339975, MTNR1A, TRIML1, TRIML2, ZFP42
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890160
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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