A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595549



Internal ID20968620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4969267..4998306hg38UCSC Ensembl
chr10:5011459..5040498hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3829040
hg1929040
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234678
Samples
Known GenesAKR1C1, AKR1C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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