A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596753



Internal ID20969824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44396809..44464672hg38UCSC Ensembl
chr19:44900972..44968894hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3867864
hg1967923
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246970
Samples
Known GenesZNF229, ZNF285
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596753
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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