A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593310



Internal ID20966381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29384765..30593038hg38UCSC Ensembl
chr10:29673694..30881967hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381208274
hg191208274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n223
Supporting Variantsnssv18221360
Samples
Known GenesKIAA1462, MAP3K8, MIR604, MIR7162, MIR938, MTPAP, PTCHD3P1, SVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593310
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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