A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563301



Internal ID20936372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70662853..70663353hg38UCSC Ensembl
chr4:71528570..71529070hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5328n223
Supporting Variantsnssv18265951
Samples
Known GenesIGJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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