A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593765



Internal ID21785808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60076784..60076784hg38UCSC Ensembl
chr10:61836542..61836542hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099261
Supporting Variants
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593765
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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