A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591556



Internal ID20964627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21101301..21842530hg38UCSC Ensembl
chr10:21390230..22131459hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38741230
hg19741230
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234433
Samples
Known GenesC10orf113, CASC10, DNAJC1, MIR1915, MLLT10, NEBL, NEBL-AS1, SKIDA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591556
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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