A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249216



Internal ID20816256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101361683..104587052hg38UCSC Ensembl
chr1:101827239..105129674hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg383225370
hg193302436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547529
Supporting Variants
Samples
Known GenesACTG1P4, AMY1A, AMY1B, AMY1C, AMY2A, AMY2B, COL11A1, DNAJA1P5, LOC100129138, LOC101928436, OLFM3, RNPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249216
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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