A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866698



Internal ID22641633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121562408..121569282hg38UCSC Ensembl
chr7:121202462..121209336hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg386875
hg196875
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866698
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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