A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412531



Internal ID21070084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90845119..90928862hg38UCSC Ensembl
chr5:90140936..90224679hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3883744
hg1983744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214998
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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