A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908260



Internal ID22683470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53698952..53709757hg38UCSC Ensembl
chr7:53766645..53777450hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3810806
hg1910806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431722
Samples
Known GenesFLJ45974
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908260
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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