A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964066



Internal ID22739001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:33155705..33155705hg38UCSC Ensembl
chr7:33195317..33195317hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430591
Samples
Known GenesBBS9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964066
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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