A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566187



Internal ID20939258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94653003..94654068hg38UCSC Ensembl
chr5:93988708..93989773hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267727
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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