A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572971



Internal ID20946042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135595980..135596712hg38UCSC Ensembl
chr7:135280728..135281460hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272606
Samples
Known GenesNUP205
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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