A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530637



Internal ID20903998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5562781..5581092hg38UCSC Ensembl
chr19:5562792..5581103hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3818312
hg1918312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199637
Samples
Known GenesTINCR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530637
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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