A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571080



Internal ID20944151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81453251..81453668hg38UCSC Ensembl
chr5:80749070..80749487hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269006
Samples
Known GenesSSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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