A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570364



Internal ID20943435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87365303..87365723hg38UCSC Ensembl
chr7:86994619..86995039hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276832
Samples
Known GenesCROT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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