A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955934



Internal ID22731127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86725016..86725016hg38UCSC Ensembl
chr7:86354332..86354332hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440370
Samples
Known GenesGRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955934
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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