A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589134



Internal ID20962205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73157255..73157530hg38UCSC Ensembl
chr10:74917013..74917288hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230320
Samples
Known GenesECD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589134
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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