A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145654



Internal ID344859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32156874..32200874hg38UCSC Ensembl
chr15:32449075..32493075hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3844001
hg1944001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701820
Samples
Known GenesCHRNA7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145654
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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