A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187302



Internal ID21326135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42349578..42349578hg38UCSC Ensembl
chr21:43769687..43769687hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954265
Supporting Variants
SamplesHG002
Known GenesTFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187302
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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