A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922830



Internal ID22698055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15815301..15816433hg38UCSC Ensembl
chr7:15854926..15856058hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg381133
hg191133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922830
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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