A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197440



Internal ID22347324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56693472..56693571hg38UCSC Ensembl
chr4:57559638..57559737hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312987, nssv14312986
SamplesNA19238, NA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197440
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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