A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv922n106



Internal ID20160279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20703761..20704561hg38UCSC Ensembl
chr13:21277900..21278700hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126339, nsv1121863
SamplesKWS1, KWS2
Known GenesIL17D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv922n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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