A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184421



Internal ID21323230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57969305..57969305hg38UCSC Ensembl
chr17:56046666..56046666hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949104
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184421
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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