A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582633



Internal ID20955704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55284661..55330469hg38UCSC Ensembl
chr15:55576859..55622667hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3845809
hg1945809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241037
Samples
Known GenesPIGB, RAB27A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582633
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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