A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544696



Internal ID20917933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185182927..185183462hg38UCSC Ensembl
chr1:185152059..185152594hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249538
Samples
Known GenesSWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544696
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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