A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv60n106



Internal ID20159417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23929910..24036610hg38UCSC Ensembl
chr1:24256400..24363100hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38106701
hg19106701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121756, nsv1142756
SamplesKWS2, KWS1
Known GenesPNRC2, SRSF10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv60n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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