A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544577



Internal ID20917816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245486831..245767897hg38UCSC Ensembl
chr1:245650133..245931199hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38281067
hg19281067
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251445
Samples
Known GenesKIF26B, SMYD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544577
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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