A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605145



Internal ID21797192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96450833..96450921hg38UCSC Ensembl
chr14:96917170..96917258hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039549
Supporting Variants
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605145
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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