A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769828



Internal ID18961490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3181802..3181925hg38UCSC Ensembl
chr1:3098366..3098489hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071333
Supporting Variants
SamplesKWP1
Known GenesPRDM16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769828
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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