A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574849



Internal ID20947920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78662724..78664351hg38UCSC Ensembl
chr7:78292040..78293667hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381628
hg191628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276664
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574849
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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