A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846779



Internal ID22621714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:61071231..61088604hg38UCSC Ensembl
chr7:61054332..61071329hg19UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg3817374
hg1916998
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508343, nssv17500581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846779
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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