A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260723



Internal ID20469941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80090157..80090222hg38UCSC Ensembl
chr17:78063956..78064021hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731259
Supporting Variants
Samples
Known GenesCCDC40
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260723
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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