A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404373



Internal ID21061926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163428366..163472178hg38UCSC Ensembl
chr5:162855372..162899184hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3843813
hg1943813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215961
Samples
Known GenesCCNG1, HMMR, NUDCD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404373
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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