A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562527



Internal ID20935598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:118953340..118954819hg38UCSC Ensembl
chr3:118672187..118673666hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg381480
hg191480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4988n223
Supporting Variantsnssv18261740
Samples
Known GenesIGSF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562527
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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