A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964660



Internal ID22739595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128357237..128357237hg38UCSC Ensembl
chr7:127997291..127997291hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430479
Samples
Known GenesPRRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964660
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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