A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517055



Internal ID20890416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10064460..10065462hg38UCSC Ensembl
chr19:10175136..10176138hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044270
Samples
Known GenesC3P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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