A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576301



Internal ID20949372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96469222..96469818hg38UCSC Ensembl
chr14:96935559..96936155hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238396
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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