A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271425



Internal ID20838465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3989923..3990457hg38UCSC Ensembl
chr6:3990157..3990691hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567152
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271425
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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