A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894861



Internal ID22669937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55350125..55350259hg38UCSC Ensembl
chr4:56216292..56216426hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415798
Samples
Known GenesSRD5A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894861
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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