A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571184



Internal ID20944255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53559611..53559773hg38UCSC Ensembl
chr6:53424409..53424571hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571184
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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