A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852495



Internal ID22627430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100086158..100087733hg38UCSC Ensembl
chr7:99683781..99685356hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381576
hg191576
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852495
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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