A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576935



Internal ID20950006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:807000..1147957hg38UCSC Ensembl
chr10:852940..1193897hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38340958
hg19340958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv598n223
Supporting Variantsnssv18226684
Samples
Known GenesGTPBP4, IDI1, IDI2, IDI2-AS1, LARP4B, WDR37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576935
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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