A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578777



Internal ID20951848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4977036..4990816hg38UCSC Ensembl
chr10:5019228..5033008hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3813781
hg1913781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv603n223
Supporting Variantsnssv18227213
Samples
Known GenesAKR1C1, AKR1C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578777
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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