A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573458



Internal ID20946529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142168365..142169164hg38UCSC Ensembl
chr7:141868165..141868964hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573458
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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