A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558866



Internal ID20931937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95223397..95224531hg38UCSC Ensembl
chr5:94559101..94560235hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381135
hg191135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267738
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558866
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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