A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526988



Internal ID22396372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25822448..25822774hg38UCSC Ensembl
chr1:26148939..26149265hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355321
SamplesNA19239
Known GenesLOC646471, MTFR1L
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526988
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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