A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372308



Internal ID22597977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8432347..8432347hg38UCSC Ensembl
chr17:8335665..8335665hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372308
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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