A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189627



Internal ID21328476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114306315..114306315hg38UCSC Ensembl
chr10:116066074..116066074hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938204
Supporting Variants
SamplesHG002
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189627
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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