A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540354



Internal ID20913644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35079912..35080616hg38UCSC Ensembl
chr1:35545513..35546217hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250901
Samples
Known GenesZMYM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540354
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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