A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861034



Internal ID22635969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134629044..134639243hg38UCSC Ensembl
chr7:134313796..134323995hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861034
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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