A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070709



Internal ID18976577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68396860..68397761hg38UCSC Ensembl
chr15:68689199..68690100hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771086
SamplesKWP1
Known GenesITGA11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070709
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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