A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950710



Internal ID16952897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:47431929..47447128hg38UCSC Ensembl
Outerchr1:47897601..47912800hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3815200
hg1915200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997147
SamplesBILGI_BIOE
Known GenesFOXD2, FOXD2-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950710
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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