A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591442



Internal ID20964513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35026727..35027319hg38UCSC Ensembl
chr14:35495933..35496525hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227158
Samples
Known GenesSRP54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591442
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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