A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564989



Internal ID20938060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27880588..27890744hg38UCSC Ensembl
chr4:27882210..27892366hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3810157
hg1910157
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564989
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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