A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549987



Internal ID20923138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91225961..91227365hg38UCSC Ensembl
chr1:91691518..91692922hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381405
hg191405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549987
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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