A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550692



Internal ID20923832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61604229..61605678hg38UCSC Ensembl
chr3:61589903..61591352hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381450
hg191450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262216
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550692
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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