A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144730



Internal ID19249890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:32169399..32184099hg38UCSC Ensembl
Outerchr15:32461600..32476300hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3814701
hg1914701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981319
SamplesKWS1
Known GenesCHRNA7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144730
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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