A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895216



Internal ID22670295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56770624..56771615hg38UCSC Ensembl
chr4:57636790..57637781hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895216
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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