A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520843



Internal ID21845202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37535235..37535235hg38UCSC Ensembl
chr1:38000836..38000836hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056963
Supporting Variants
Samples
Known GenesSNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520843
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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