A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965439



Internal ID22740374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40968011..40968011hg38UCSC Ensembl
chr7:41007610..41007610hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445275
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965439
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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