A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860849



Internal ID22635784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97321177..97326126hg38UCSC Ensembl
chr7:96950489..96955438hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384950
hg194950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860849
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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