A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537599



Internal ID20910935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101583371..101583932hg38UCSC Ensembl
chr3:101302215..101302776hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259473
Samples
Known GenesPCNP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537599
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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