A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568512



Internal ID20941583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32472896..32473362hg38UCSC Ensembl
chr7:32512508..32512974hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568512
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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