A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400602



Internal ID21058155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77626801..77629500hg38UCSC Ensembl
chr5:76922626..76925325hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214142
Samples
Known GenesOTP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400602
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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