A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599503



Internal ID20972574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36692905..37122559hg38UCSC Ensembl
chr19:37183807..37613461hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38429655
hg19429655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3502n223
Supporting Variantsnssv18247709
Samples
Known GenesZNF345, ZNF420, ZNF567, ZNF568, ZNF790, ZNF790-AS1, ZNF829, ZNF850
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599503
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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