A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562649



Internal ID20935720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42386747..42387605hg38UCSC Ensembl
chr7:42426346..42427204hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562649
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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