A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571489



Internal ID20944560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41996151..41997013hg38UCSC Ensembl
chr4:41998168..41999030hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264633
Samples
Known GenesSLC30A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571489
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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