A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526873



Internal ID22396256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183642190..183642441hg38UCSC Ensembl
chr4:184563343..184563594hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316767, nssv14316765, nssv14316768, nssv14316766, nssv14316770, nssv14316764, nssv14316769
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00733, HG00514
Known GenesRWDD4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526873
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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