A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441079



Internal ID22498949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117691003..117691003hg38UCSC Ensembl
chr7:117331057..117331057hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950195
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441079
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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