A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397674



Internal ID21055227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90736601..90738200hg38UCSC Ensembl
chr5:90032418..90034017hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133751
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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