A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151347



Internal ID19201798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143845906..143862007hg38UCSC Ensembl
Outerchr7:143542999..143559100hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3816102
hg1916102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003911
SamplesKWB1
Known GenesFAM115A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151347
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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