A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565370



Internal ID20938441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68996961..69126451hg38UCSC Ensembl
chr4:69862679..69992169hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38129491
hg19129491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265915
Samples
Known GenesUGT2B10, UGT2B7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565370
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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