A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846563



Internal ID22621498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21489252..21508871hg38UCSC Ensembl
chr7:21528870..21548489hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3819620
hg1919620
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504749
Samples
Known GenesSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846563
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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