A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550411



Internal ID20923557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92565969..92566828hg38UCSC Ensembl
chr1:93031526..93032385hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38860
hg19860
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv266n223
Supporting Variantsnssv18252701
Samples
Known GenesEVI5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550411
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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