A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152142



Internal ID18850590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:147145889..147145955hg38UCSC Ensembl
Outerchr7:146842981..146843047hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996749
SamplesKWB1
Known GenesCNTNAP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152142
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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