A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069856



Internal ID18979054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41621801..41622302hg38UCSC Ensembl
chr15:41913999..41914500hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767084
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069856
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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