A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253929



Internal ID20820969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84983478..84984772hg38UCSC Ensembl
chr1:85449161..85450455hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381295
hg191295
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536601
Supporting Variants
Samples
Known GenesMCOLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253929
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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