A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567948



Internal ID20941019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127296233..127296974hg38UCSC Ensembl
chr6:127617378..127618119hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271187
Samples
Known GenesECHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567948
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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