A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142580



Internal ID341781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10000..38000hg38UCSC Ensembl
chr7:10001..38000hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3828001
hg1928000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142580
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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