A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv64n106



Internal ID19018173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25283609..25287809hg38UCSC Ensembl
chr1:25610100..25614300hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384201
hg194201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118431, nsv1115341
SamplesKWS1, KWS2
Known GenesRHD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv64n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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