A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv630n106



Internal ID19018739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43887987..43888363hg38UCSC Ensembl
chr11:43909537..43909913hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121475, nsv1141138
SamplesKWS1, KWS2
Known GenesALKBH3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv630n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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