A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926325



Internal ID22701552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100126046..100145306hg38UCSC Ensembl
chr7:99723669..99742929hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3819261
hg1919261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442692
Samples
Known GenesMBLAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926325
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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