A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567257



Internal ID20940328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44815347..44816015hg38UCSC Ensembl
chr7:44854946..44855614hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567257
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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