A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949974



Internal ID17298848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143845208..143852507hg38UCSC Ensembl
Outerchr7:143542301..143549600hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998615
SamplesBILGI_BIOE
Known GenesFAM115A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949974
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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