A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846586



Internal ID22621521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37653973..37665516hg38UCSC Ensembl
chr7:37693576..37705119hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3811544
hg1911544
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506337
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846586
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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