A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597785



Internal ID20970856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16909494..16909898hg38UCSC Ensembl
chr19:17020304..17020708hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247575
Samples
Known GenesCPAMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597785
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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