A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565071



Internal ID20938142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94625078..94625390hg38UCSC Ensembl
chr5:93960783..93961095hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267726
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565071
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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