A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577393



Internal ID20950464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7017624..7018391hg38UCSC Ensembl
chr11:7038855..7039622hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv966n223
Supporting Variantsnssv18224496
Samples
Known GenesZNF214
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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