A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521188



Internal ID20894549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4266895..4287678hg38UCSC Ensembl
chr19:4266892..4287675hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3820784
hg1920784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046418
Samples
Known GenesCCDC94, SHD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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