A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547529



Internal ID20920730
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 StatusM
Merged Variants
Supporting Variantsnssv18249216
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)nsv6547529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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