A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140977



Internal ID340171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186008703..186213068hg38UCSC Ensembl
chr4:186929857..187134222hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38204366
hg19204366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961264
Samples
Known GenesCYP4V2, FAM149A, FLJ38576, TLR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140977
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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