A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546491



Internal ID20919707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29225999..29227029hg38UCSC Ensembl
chr1:29552511..29553541hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252367
Samples
Known GenesMECR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546491
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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