A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516088



Internal ID20889449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56793401..56797600hg38UCSC Ensembl
chr19:57304769..57308968hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199690
Samples
Known GenesZIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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