A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847548



Internal ID22622483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9255927..9260984hg38UCSC Ensembl
chr7:9295557..9300614hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg385058
hg195058
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847548
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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