A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910915



Internal ID22686127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69048298..69048603hg38UCSC Ensembl
chr7:68513285..68513590hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910915
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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