A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557136



Internal ID20930207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119632604..119634220hg38UCSC Ensembl
chr8:120644844..120646460hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381617
hg191617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277078
Samples
Known GenesENPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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