A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545842



Internal ID20919066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64066501..64067285hg38UCSC Ensembl
chr1:64532173..64532957hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250608
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545842
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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