A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587949



Internal ID20961020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100283289..100284973hg38UCSC Ensembl
chr10:102043046..102044730hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg381685
hg191685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221857
Samples
Known GenesBLOC1S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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