A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377799



Internal ID22435669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43958135..43958135hg38UCSC Ensembl
chr17:42035503..42035503hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979457
Supporting Variants
Samples
Known GenesPYY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377799
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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