A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572964



Internal ID20946035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8327069..8334318hg38UCSC Ensembl
chr9:8327069..8334318hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg387250
hg197250
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7563n223
Supporting Variantsnssv18281206
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572964
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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