A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892986



Internal ID22668043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177435913..177441610hg38UCSC Ensembl
chr5:176862914..176868611hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg385698
hg195698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425127
Samples
Known GenesGRK6, PRR7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892986
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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