A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564771



Internal ID20937842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103328096..103328473hg38UCSC Ensembl
chr7:102968543..102968920hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272188
Samples
Known GenesDNAJC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564771
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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