A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704206



Internal ID127872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64539628..64543567hg38UCSC Ensembl
chr15:64831827..64835766hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383940
hg193940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515368
Supporting Variants
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704206
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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