A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184409



Internal ID21323217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10107404..10107404hg38UCSC Ensembl
chr17:10010721..10010721hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942135
Supporting Variants
SamplesHG002
Known GenesGAS7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184409
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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