A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142842



Internal ID342043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61785368..61976000hg38UCSC Ensembl
chr9:44958294..45112152hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38190633
hg19153859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023040
Samples
Known GenesFAM27C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142842
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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