A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714660



Internal ID138326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75786630..75787678hg38UCSC Ensembl
chr17:73782711..73783759hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528781
Supporting Variants
Samples
Known GenesUNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714660
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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