A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145618



Internal ID344823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83207000..83224000hg38UCSC Ensembl
chr17:81154769..81171769hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3817001
hg1917001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145618
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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