A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546070



Internal ID20919290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25315127..25377381hg38UCSC Ensembl
chr1:25641618..25703872hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3862255
hg1962255
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251554
Samples
Known GenesRHCE, RHD, TMEM50A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546070
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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