A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899628



Internal ID22674759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6812721..6820715hg38UCSC Ensembl
chr4:6814448..6822442hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg387995
hg197995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423699
Samples
Known GenesKIAA0232
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899628
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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