A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860155



Internal ID22635090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129560283..129565410hg38UCSC Ensembl
chr7:129200124..129205251hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg385128
hg195128
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860155
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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