A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855441



Internal ID22630376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139553269..139555195hg38UCSC Ensembl
chr7:139238015..139239941hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381927
hg191927
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855441
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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