A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554135



Internal ID20927242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77645984..77646268hg38UCSC Ensembl
chr1:78111669..78111953hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253156
Samples
Known GenesZZZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554135
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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