A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557243



Internal ID20930314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23447487..23448522hg38UCSC Ensembl
chr7:23487106..23488141hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381036
hg191036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272702
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557243
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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