A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949156



Internal ID22724609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128307472..128307472hg38UCSC Ensembl
chr7:127947525..127947525hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433574
Samples
Known GenesMGC27345
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949156
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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