A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145696



Internal ID344901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19149555..19237111hg38UCSC Ensembl
chr17:19052868..19140424hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3887557
hg1987557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711993
Samples
Known GenesGRAPL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145696
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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