A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151641



Internal ID19203290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:34059038..34059174hg38UCSC Ensembl
Outerchr15:34351239..34351375hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003064
SamplesKWB1
Known GenesCHRM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151641
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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