A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575386



Internal ID20948457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139314663..139316079hg38UCSC Ensembl
chr7:138999409..139000825hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381417
hg191417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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