A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604596



Internal ID20977667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108152701..108183000hg38UCSC Ensembl
chr6:108473905..108504204hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3830300
hg1930300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216783
Samples
Known GenesNR2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604596
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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