A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412324



Internal ID22470194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102757305..102757630hg38UCSC Ensembl
chr4:103678462..103678787hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904915
Supporting Variants
Samples
Known GenesMANBA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412324
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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