A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249872



Internal ID20816913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117397842..117398542hg38UCSC Ensembl
chr1:117940464..117941164hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537860
Supporting Variants
Samples
Known GenesMAN1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249872
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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