A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857169



Internal ID22632104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156381601..156382800hg38UCSC Ensembl
chr7:156174295..156175494hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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