A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265032



Internal ID20832072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2853640..2854306hg38UCSC Ensembl
chr4:2855367..2856033hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558388
Supporting Variants
Samples
Known GenesADD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265032
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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