A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070616



Internal ID19316166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110906991..110907298hg38UCSC Ensembl
chr13:111559338..111559645hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769357
SamplesKWP1
Known GenesANKRD10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070616
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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