A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4004n106



Internal ID22797832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64455114..64476244hg38UCSC Ensembl
chr9:43020700..43041800hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3821131
hg1921101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1125032, nsv1129001
SamplesKWS2, KWS1
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4004n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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