A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532706



Internal ID20906067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51168346..51212096hg38UCSC Ensembl
chr19:51671603..51715352hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3843751
hg1943750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198298
Samples
Known GenesMIR8074, SIGLEC17P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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