A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526685



Internal ID22396068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37124301..37124358hg38UCSC Ensembl
chr4:37125923..37125980hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314865, nssv14314864
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526685
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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