A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000665



Internal ID21910008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91408419..91408605hg38UCSC Ensembl
chr5:90704236..90704422hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549782
Samples
Known GenesARRDC3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000665
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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