A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865466



Internal ID22640401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128290816..128307872hg38UCSC Ensembl
chr7:127930869..127947925hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3817057
hg1917057
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509632
Samples
Known GenesMGC27345
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865466
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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