A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925601



Internal ID22700828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155226046..155227287hg38UCSC Ensembl
chr7:155017756..155018997hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1947n209
Supporting Variantsnssv17440891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925601
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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