A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192157



Internal ID21331028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117126450..117126450hg38UCSC Ensembl
chr10:118885961..118885961hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3955149
Supporting Variants
SamplesHG002
Known GenesKIAA1598
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192157
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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