A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1415n106



Internal ID20160772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9161898..9162015hg38UCSC Ensembl
chr17:9065215..9065332hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126209, nsv1130477
SamplesKWS1
Known GenesNTN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1415n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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