A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866271



Internal ID22641206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74617951..74618954hg38UCSC Ensembl
chr7:74032270..74033268hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381004
hg19999
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509305, nssv17502789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866271
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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