A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250949



Internal ID20817989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40728301..40728786hg38UCSC Ensembl
chr1:41193973..41194458hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543565
Supporting Variants
Samples
Known GenesNFYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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