A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1499n106



Internal ID20160856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67731238..67731532hg38UCSC Ensembl
chr17:65727354..65727648hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135506, nsv1111525, nsv1126265
SamplesKWS1, KWS2
Known GenesNOL11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1499n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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