A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920555



Internal ID22695778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81669921..81694878hg38UCSC Ensembl
chr7:81299237..81324194hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3824958
hg1924958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920555
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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