A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598377



Internal ID20971448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37679174..37873702hg38UCSC Ensembl
chr19:38170075..38364342hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38194529
hg19194268
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248337
Samples
Known GenesLOC100631378, LOC644554, ZNF573, ZNF607, ZNF781
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598377
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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