A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530768



Internal ID20904129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37643067..37675359hg38UCSC Ensembl
chr19:38133968..38166260hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3832293
hg1932293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046665
Samples
Known GenesZFP30, ZNF781
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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