A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003911



Internal ID19188497
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 StatusS
Merged Variantsnsv1151347
Supporting Variants
SamplesKWB1
Known GenesFAM115A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003911
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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