A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572501



Internal ID20945572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138986543..138987134hg38UCSC Ensembl
chr7:138671289..138671880hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7130n223
Supporting Variantsnssv18274397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572501
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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