A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544259



Internal ID20917498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70313247..70314399hg38UCSC Ensembl
chr1:70778930..70780082hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251340
Samples
Known GenesANKRD13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544259
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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