A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857690



Internal ID22632625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90336135..90338102hg38UCSC Ensembl
chr7:89965449..89967416hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381968
hg191968
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857690
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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