A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151834



Internal ID18853005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152277814..152284315hg38UCSC Ensembl
Outerchr7:151974899..151981400hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386502
hg196502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999013
SamplesKWB1
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151834
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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