A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572912



Internal ID20945983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66044866..66046161hg38UCSC Ensembl
chr7:65509853..65511148hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572912
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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