A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153578



Internal ID19195689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82882813..82888919hg38UCSC Ensembl
Outerchr15:83551565..83557671hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386107
hg196107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002233
SamplesKWB1
Known GenesHOMER2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153578
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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