A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714942



Internal ID138608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79692216..79707723hg38UCSC Ensembl
chr17:77666146..77681532hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3815508
hg1915387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521222
Supporting Variants
Samples
Known GenesMIR4739
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714942
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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