A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595270



Internal ID20968341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49140132..49141437hg38UCSC Ensembl
chr15:49432329..49433634hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381306
hg191306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2532n223
Supporting Variantsnssv18238058
Samples
Known GenesCOPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595270
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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