A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556365



Internal ID20929436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103150999..103151698hg38UCSC Ensembl
chr7:102791446..102792145hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7040n223
Supporting Variantsnssv18271597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556365
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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