A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847520



Internal ID22622455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7576269..7581155hg38UCSC Ensembl
chr7:7615900..7620786hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg384887
hg194887
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502835
Samples
Known GenesMIOS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847520
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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