A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557490



Internal ID20930561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11235349..11384688hg38UCSC Ensembl
chr4:11236973..11386312hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38149340
hg19149340
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263610
Samples
Known GenesMIR572
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557490
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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