A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv21n106



Internal ID19018130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3725236..3726436hg38UCSC Ensembl
chr1:3641800..3643000hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1136061, nsv1142743
SamplesKWS1, KWS2
Known GenesTP73
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv21n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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