A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581963



Internal ID20955034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33029341..33029973hg38UCSC Ensembl
chr11:33050887..33051519hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1019n223
Supporting Variantsnssv18223200
Samples
Known GenesDEPDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581963
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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