A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546790



Internal ID20920000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100641361..100847343hg38UCSC Ensembl
chr1:101106917..101312899hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38205983
hg19205983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249198
Samples
Known GenesLOC100128787, VCAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546790
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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