A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556611



Internal ID329745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37882362..37897638hg38UCSC Ensembl
chr6:37850138..37865414hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3815277
hg1915277
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980600
Samples
Known GenesZFAND3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556611
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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