A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908956



Internal ID22684166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2495395..2497533hg38UCSC Ensembl
chr7:2535029..2537167hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382139
hg192139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908956
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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