A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563717



Internal ID20936788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84132837..84134046hg38UCSC Ensembl
chr7:83762153..83763362hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381210
hg191210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276774
Samples
Known GenesSEMA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563717
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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