A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546593



Internal ID20919803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10003178..10003946hg38UCSC Ensembl
chr1:10063236..10064004hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249175
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546593
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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