A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552000



Internal ID20925131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61191960..61192712hg38UCSC Ensembl
chr1:61657632..61658384hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250460
Samples
Known GenesNFIA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552000
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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