A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153812



Internal ID18852240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152401614..152416615hg38UCSC Ensembl
Outerchr7:152098699..152113700hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3815002
hg1915002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002465
SamplesKWB1
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153812
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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