A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1017n106



Internal ID20160374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96695580..96695692hg38UCSC Ensembl
chr13:97347834..97347946hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1139555, nsv1130090
SamplesKWS1
Known GenesHS6ST3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1017n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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