A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152566



Internal ID18850971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:146902807..146908708hg38UCSC Ensembl
Outerchr7:146599899..146605800hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385902
hg195902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999745
SamplesKWB1
Known GenesCNTNAP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152566
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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