A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859145



Internal ID22634080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149264758..149267761hg38UCSC Ensembl
chr7:148961849..148964852hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383004
hg193004
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502627
Samples
Known GenesZNF783
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859145
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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