A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548972



Internal ID20922150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35100511..35100889hg38UCSC Ensembl
chr1:35566112..35566490hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250903
Samples
Known GenesZMYM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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