A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071110



Internal ID19325713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71864067..71870462hg38UCSC Ensembl
chr13:72438199..72444600hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg386396
hg196402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762819
SamplesKWP1
Known GenesDACH1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071110
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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