A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412107



Internal ID22469977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16076570..16077642hg38UCSC Ensembl
chr4:16078193..16079265hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381073
hg191073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897413
Supporting Variants
Samples
Known GenesPROM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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