A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555886



Internal ID20928957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4116261..4116764hg38UCSC Ensembl
chr6:4116495..4116998hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271439
Samples
Known GenesC6orf201, ECI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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