A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142008



Internal ID341208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74766000..74774779hg38UCSC Ensembl
chr7:74180345..74189126hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg388780
hg198782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001003
Samples
Known GenesNCF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142008
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer