A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907856



Internal ID22683066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90556333..90592093hg38UCSC Ensembl
chr7:90185647..90221407hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3835761
hg1935761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907856
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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