A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906320



Internal ID22681519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56912715..56912998hg38UCSC Ensembl
chr4:57778881..57779164hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412648
Samples
Known GenesREST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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