A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553442



Internal ID20926550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60505721..60517414hg38UCSC Ensembl
chr1:60971393..60983086hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3811694
hg1911694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553442
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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