A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431147



Internal ID22489017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27278222..27278222hg38UCSC Ensembl
chr7:27317841..27317841hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431147
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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