A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563277



Internal ID20936348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96453266..96453639hg38UCSC Ensembl
chr7:96082578..96082951hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563277
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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