A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071582



Internal ID18969946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25340930..25342331hg38UCSC Ensembl
chr2:25563799..25565200hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3761971
SamplesKWP1
Known GenesDNMT3A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071582
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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