A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141900



Internal ID341099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142748779..142762779hg38UCSC Ensembl
chr7:142456630..142470628hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3814001
hg1913999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006395
Samples
Known GenesPRSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141900
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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