A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526202



Internal ID22395582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35391781..35391914hg38UCSC Ensembl
chr1:35857382..35857515hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361595, nssv14361594
SamplesNA19238, NA19240
Known GenesZMYM4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526202
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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