A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612195



Internal ID21804242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60978580..60978580hg38UCSC Ensembl
chr15:61270779..61270779hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087633
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612195
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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