A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597430



Internal ID20970501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39976209..39976874hg38UCSC Ensembl
chr19:40482116..40482781hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248403
Samples
Known GenesPSMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597430
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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