A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854380



Internal ID22629315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91625187..91631071hg38UCSC Ensembl
chr7:91254502..91260386hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg385885
hg195885
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854380
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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