A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398449



Internal ID21056002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76315166..76351194hg38UCSC Ensembl
chr5:75610991..75647019hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3836029
hg1936029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216582
Samples
Known GenesSV2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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