A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148710



Internal ID18851342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:58620663..58620941hg38UCSC Ensembl
Outerchr15:58912862..58913140hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997498
SamplesKWB1
Known GenesADAM10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148710
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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