A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556697



Internal ID20929768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147821823..147825767hg38UCSC Ensembl
chr4:148742974..148746918hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg383945
hg193945
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264820
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556697
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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