A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910179



Internal ID22685389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98140130..98140196hg38UCSC Ensembl
chr7:97769442..97769508hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440717
Samples
Known GenesLMTK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910179
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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