A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272739



Internal ID20839779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24290560..24366474hg38UCSC Ensembl
chr7:24330179..24406093hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3875915
hg1975915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556044
Supporting Variants
Samples
Known GenesNPY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272739
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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