A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575903



Internal ID20948974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39110827..39111391hg38UCSC Ensembl
chr14:39580031..39580595hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2104n223
Supporting Variantsnssv18221370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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