A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950205



Internal ID17299079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:91449044..91459143hg38UCSC Ensembl
Outerchr1:91914601..91924700hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997173
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950205
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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